Tag: M.W=100-150

Mastagli, Pierre published the artcileCatalytic transketalizations in the presence of metallic oxides, Product Details of C6H12O2, the publication is Compt. Rend. (1963), 257(3), 690-2, database is CAplus.

Me₂C(OEt)₂ (I) (0.2 mol), 0.5 mol ROH (R = alkyl), and 10% catalyst was refluxed 2 h., filtered, and fractionated to give Me₂C(OR)₂ (II). I and heptanol gave II (R = C₇H₁₅) (catalyst and % yield given): MoO₃, 17; Amberlite IR 120, 12; Co₂O₃Co₃O₄ mixture, 10; WO₃, 1. Using MoO₃ catalyst, the following II were prepared (R, b.p./mm., n_D/temperature, % yield given): Bu, 130°, 1.414/18°, 19; C₅H₁₁, 112°/15, 1.4188/17°, 46; C₇H₁₅, 160°/10, 1.4319/17°, 17; C₈H₁₇, 185°/13, 1.4347/19° 15; sec-C₈H₁₇ 165°/10, 1.4358/20°, 5; C₁₂H₂₅, 240°/12 (m. 35°), -, 10. Traces of byproduct MeC(:CH₂)OR were usually formed, but with C₁₂H₂₅OH, appreciable amounts of MeC(:CH₂)OC₁₂H₂₅, b₁₂ 195°, n¹⁵_D 1.4469, formed, which was reduced by Raney Ni and H to iso-PrOC₁₂H₂₅, b₁₀ 138°, n²⁰_D 1.4290. Good yields of ketals (structure not given), without formation of byproducts, were obtained from diols and I with MoO₃ catalyst (diol, product formula, b.p., n_D/temperature, % yield given): MeCH(OH)CH₂OH, C₆H₁₂O₂, b. 99°, 1.4038/16.5°, 43; (HOCH₂)₂CH₂, C₆H₁₂O₂, b. 124°, 1.4196/19°, 65; MeCH(OH)CH₂CH₂OH, C₇H₁₄O₂, b. 131°, 1.4190/19.7°, 76; (HOCH₂CH₂)₂, C₇H₁₄O₂, b. 136°, 1.4277/18°, 38; HOCH₂CMePrCH₂OH, C₁₀H₂₀O₂, b₁₀ 71°, 1.4320/20°, 70.

Compt. Rend. published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Product Details of C6H12O2.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Zhu, Zuolin published the artcileOrganometallic Catalysis: Formation of 1,3-Dioxolanes and Their Analogs Catalyzed by Methylrhenium Trioxide (MTO), Name: 2,2,4-Trimethyl-1,3-dioxolane, the publication is Organometallics (1997), 16(16), 3658-3663, database is CAplus.

Methylrhenium trioxide (MTO) catalyzes several cycloaddition reactions. 1,3-Dioxolanes were obtained in good yields from the reactions of epoxides with aldehydes or ketones; the geometric configuration of the epoxide substituents remains unchanged in the product, which was shown to be the consequence of two configuration inversions in sequence. The independently known bis(alkoxy)rhenium complex formed from MTO and the epoxide is an intermediate that could be detected at a low level during the reaction; indeed, its formation limits the rate of the overall reaction. Related cycloaddition reactions are the formation of ketene acetals from diphenylketene and epoxides and of oxazolidines from aromatic imines and epoxides, both MTO-catalyzed.

Organometallics published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C10H9NO, Name: 2,2,4-Trimethyl-1,3-dioxolane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Tateo, Fernando published the artcileIdentification of 1,3-dioxolanes in coffee-like flavorings, Recommanded Product: 2,2,4-Trimethyl-1,3-dioxolane, the publication is Journal of High Resolution Chromatography (1998), 21(12), 658-660, database is CAplus.

Com. available coffee-like flavoring preparations, identifying certain dioxolane structures of particular interest were concerned. The research was carried out by GC/MS, and spectral characterization was performed of the compounds in question, and especially of the acetals and ketals produced from compounds with carbonyl functions and 1,2-propylene glycol. Some determinations by chiral gas chromatog. and by isotope ratio mass spectrometry (IRMS) were useful in improving the anal. characterization of certain dioxolanes.

Journal of High Resolution Chromatography published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C10H18O, Recommanded Product: 2,2,4-Trimethyl-1,3-dioxolane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Barker, S. A. published the artcileSpectra of acetals. I. The infrared and Raman spectra of 1,3-dioxolane, Application In Synthesis of 1193-11-9, the publication is Journal of the Chemical Society (1959), 802-6, database is CAplus.

For eventual application to the interpretation of the spectra of sugar acetals and ketals containing substituted dioxolane ring systems, the Raman and infrared spectra of 1,3-dioxolane have been measured and observed bands have been correlated with vibrational modes giving rise to them. Raman lines were measured within ± 1 cm.^-1 against standard Fe-arc lines, by using a Hilger Raman spectrometer and the exciting line 4358 A. from a Hg lamp. Qual. polarization data were obtained from exposures with Polaroid wrapped around the Raman tube. Infrared absorption spectra were measured on a Grubb-Parsons single beam spectrometer with NaCl and KBr prisms. The C-H stretching frequencies were measured in the 3rd order on a grating spectrometer having a 2500-lines/in. grating. Measurements were carried out in the vapor state, as liquid films, and as CCl₄ solutions The exact geometry of the dioxolane ring is not known but Mills (C.A. 50, 2435i) has suggested that the ring is nearly planar. However, the diffuse nature of the Raman lines and the breadth of the infrared bands indicates a puckered ring. Since the degree of puckering is probably small the symmetry will not deviate far from that of a planar ring. Application of the selection rules to such a planar ring indicates that 27 normal vibrations are expected for 1,3-dioxolane and these expected bands are shown in a table according to symmetry class. Assignments for 25 of these expected bands observed in the Raman or infrared spectra have been made. These bands and their assignments are discussed under the following headings: C-H stretching vibrations; antisym. C-H stretching; vibrations; methylene scissoring, wagging, twisting, and rocking vibrations; and ring vibrations. The 2 fundamentals to which frequencies have not been assigned are the out-of-plane ring frequencies which lie below the limit of the infrared measurements, 420 cm.^-1, and which have not been observed in the Raman effect. Assignment of frequencies has been difficult as the infrared spectrum of 1,3-dioxolane vapor does not exhibit recognizable band shapes and, for the 5 polarized lines expected below 140 cm.^-1 in Raman spectra, only 1 highly polarized line and 1 partially polarized line have been observed as polarized.

Journal of the Chemical Society published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Application In Synthesis of 1193-11-9.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Barker, S. A. published the artcileSpectra of acetals. II. Infrared and Raman spectra of substituted 1,3-dioxolanes, Safety of 2,2,4-Trimethyl-1,3-dioxolane, the publication is Journal of the Chemical Society (1959), 807-13, database is CAplus.

Infrared and Raman spectra have been reported for 9 substituted 1,3-dioxolanes: 2-methyl; 4-methyl; 2,2-dimethyl; cis-2,4-dimethyl; trans-2,4-dimethyl; 2,2,4-trimethyl; 4-hydroxymethyl-2,2-dimethyl; 4-deuterioöxymethyl-2,2-dimethyl; and 4-methoxymethyl-2,2-dimethyl. Infrared and Raman spectra of these compounds were measured. Some 100 bands observed are listed in a table with their assignments made by analogy with the assignments for dioxolane. Internal vibrations of the methyl groups were made by use of the review of Sheppard and Simpson (C.A. 47, 6767d). These assignments are discussed under the following headings: vibrations involving methylene groups; vibrations involving methyl substituents, including bending, rocking, stretching, and deformations of the methyl groups; C-H deformations; vibrations involving a hydroxymethyl substituent; and ring vibrations. The infrared spectra of the 3,4-O-isopropylidene ketals of L-iditol, D-mannitol, and D-sorbitol were measured over the range 650-1500 cm.^-1 Assignments, made by analogy with those for the substituted dioxolanes, are given.

Journal of the Chemical Society published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Safety of 2,2,4-Trimethyl-1,3-dioxolane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Sontsev, V. M. published the artcileConversion of propylene glycol-acetone mixture into 2,2,4-trimethyl-1,3-dioxolane over Dowex DR-2030 and ZrO₂-SiO₂ acid catalysts, Recommanded Product: 2,2,4-Trimethyl-1,3-dioxolane, the publication is Khimiya, Fizika ta Tekhnologiya Poverkhni (2014), 5(1), 42-46, database is CAplus.

The conversion of propylene glycol-acetone mixtures into cyclic ketal over sulforesin Dowex DR-2030 and acidic ZrO₂-SiO₂ catalysts under steady conditions at 40-100 °C has been studied. It has been shown that 2,2,4-trymethyl-1,3-dioxolane can be obtained with 99-94% yield at 40-50 °C. Conversion of propylene glycol increases from 65 to 75% when providing of the ketalization process with water removing.

Khimiya, Fizika ta Tekhnologiya Poverkhni published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C20H18BrN3, Recommanded Product: 2,2,4-Trimethyl-1,3-dioxolane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Leggetter, B. E. published the artcileInfluence of substituents on the ease and direction of ring opening in the LiAlH₄-AlCl₃ reductive cleavage of substituted 1,3-dioxolanes, Application of 2,2,4-Trimethyl-1,3-dioxolane, the publication is Canadian Journal of Chemistry (1964), 42(5), 990-1004, database is CAplus.

Room temperature hydrogenolysis by LiAlH₄-AlCl₃ of ether solutions of a number of 1,3-dioxolanes was studied. Electron-donor substituents on the C-2 atom of the ring accelerated, while electron-acceptor substituents on C-2 retarded, the reductive ring cleavage. The same effect, but to a lesser extent, was observed when these substituents were attached to the C-4 or C-5 atom of the ring. When electron-donor substituents were attached to C-4, ring cleavage occurred predominantly at the (C-2)-O bond remote from the C-4 position. On the other hand, electron-withdrawing groups attached to C-4 gave predominantly scission of the (C-2)-O bond closer to the C-4 substituted position. In contrast to this marked control over the direction of ring cleavage exhibited by substituents on C-4, those on C-2 generally had little or no effect on the direction of ring opening. A mechanistic interpretation of the results was given.

Canadian Journal of Chemistry published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Application of 2,2,4-Trimethyl-1,3-dioxolane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Magnus, Philip published the artcileLewis Acid Catalyzed α-Functionalization of Ketals for the Regioselective Synthesis of α-Carbamoyl Ketals, Related Products of dioxole, the publication is Organic Letters (2012), 14(15), 3952-3954, database is CAplus and MEDLINE.

Treatment of α-carbamoyl ketals with DEAD in the presence of BF₃·OEt₂ gave α-N,N’-dialkyldicarboxylate hydrazines, which was N-alkylated and in situ eliminated (E1cb) to give α-carbamoyl ketals.

Organic Letters published new progress about 177-10-6. 177-10-6 belongs to dioxole, auxiliary class Dioxolane,Spiro, name is 1,4-Dioxaspiro[4.5]decane, and the molecular formula is C8H14O2, Related Products of dioxole.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

Kuznetsov, V. V. published the artcileRelative activity of 1,3-dioxolanes in a reaction with pentylborodichloride, Synthetic Route of 1193-11-9, the publication is Izvestiya Vysshikh Uchebnykh Zavedenii, Khimiya i Khimicheskaya Tekhnologiya (1990), 33(3), 34-6, database is CAplus.

Reaction of equimol. amounts of dioxolanes I (R = H, Me, R¹ = H, Me, CHMe₂, heptyl, RR¹ = O; R² = R³ = H, Me, R² = H, R³ = Me) with Me(CH₂)₄BCl₂ at 20° for 4-6 h gave dioxaborolanes II (same R², R³). The degree of conversion of I was dependent on the relative thermodn. stability of the initial and final compounds

Izvestiya Vysshikh Uchebnykh Zavedenii, Khimiya i Khimicheskaya Tekhnologiya published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Synthetic Route of 1193-11-9.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem

LeBouf, Ryan F. published the artcileHeadspace analysis for screening of volatile organic compound profiles of electronic juice bulk material, Name: 2,2,4-Trimethyl-1,3-dioxolane, the publication is Analytical and Bioanalytical Chemistry (2018), 410(23), 5951-5960, database is CAplus and MEDLINE.

The use of electronic nicotine delivery systems continues to gain popularity, and there is concern for potential health risks from inhalation of aerosol and vapor produced by these devices. An anal. method was developed that provided quant. and qual. chem. information for characterizing the volatile constituents of bulk electronic cigarette liquids (e-liquids) using a static headspace technique. Volatile organic compounds (VOCs) were screened from a convenience sample of 146 e-liquids by equilibrating 1 g of each e-liquid in amber vials for 24 h at room temperature Headspace was transferred to an evacuated canister and quant. analyzed for 20 VOCs as well as tentatively identified compounds using a preconcentrator/gas chromatog./mass spectrometer system. The e-liquids were classified into flavor categories including brown, fruit, hybrid dairy, menthol, mint, none, tobacco, and other. 2,3-Butanedione was found at the highest concentration in brown flavor types, but was also found in fruit, hybrid dairy, and menthol flavor types. Benzene was observed at concentrations that are concerning given the carcinogenicity of this compound (max 1.6 ppm in a fruit flavor type). The proposed headspace anal. technique coupled with partition coefficients allows for a rapid and sensitive prediction of the volatile content in the liquid The technique does not require onerous sample preparation, dilution with organic solvents, or sampling at elevated temperatures Static headspace screening of e-liquids allows for the identification of volatile chem. constituents which is critical for identifying and controlling emission of potentially hazardous constituents in the workplace.

Analytical and Bioanalytical Chemistry published new progress about 1193-11-9. 1193-11-9 belongs to dioxole, auxiliary class Dioxolanes, name is 2,2,4-Trimethyl-1,3-dioxolane, and the molecular formula is C6H12O2, Name: 2,2,4-Trimethyl-1,3-dioxolane.

Referemce:
https://en.wikipedia.org/wiki/1,3-Benzodioxole,
Dioxole | C3H4O2 – PubChem