Likhterov, V. R. published the artcile1,3-Dioxolanes. I. Chlorination of some cyclic ketals of acetone and vicinal glycols, Product Details of C6H12O2, the publication is Zhurnal Organicheskoi Khimii (1968), 4(1), 69-72, database is CAplus.
Chlorination of 2,2,4-trimethyl-1,3-dioxolane (I), 2,2-dimethyl-4-chloromethyl-1,3-dioxolane, 2,2-dimethyl-4-methoxymethyl-1,3-dioxolane, 2,2-dimethyl-4-acetoxymethyl-1,3-dioxolane (II), and 2,2-dimethyl-1,3-dioxolane is described. The exothermic reaction was carried out with cooling at 15-20° by passing Cl through the dioxolane followed by distillation The starting dioxolanes were all known previously with the exception of II, b2 71-2°. Chlorination gave 2-chloromethyl-2-methyl-4-(R-substituted)-1,3-dioxolanes (III) (R, % yield, b.p./mm., and n20D given): Me, 73.5, 53-4°/15, 1.4352; CH2Cl, 78.3, 71-2°/2, 1.4701; MeOCH2, 71.3, 69-71°/2, 1.4486; MeCO2CH2, 72.0, 103-5°/2, 1.4535; H, 76.0, 60-3°/20, 1.4450. Alk. hydrolysis of III (R = MeCO2CH2) gave III (R = CH2OH), b3 96-8°, n20D 1.4688 (containing 46-50% cis- and 50-4% trans-isomer). Reaction of III (R = CH2Cl) with MeCO2K gave III (R = MeCO2CH2). Action of PCl5 on III (R = CH2OH) gave III (R = CH2Cl). Hydrolysis of III gave MeCOCH2Cl, identified by the m.p. of its 2,4-dinitrophenylhydrazone derivative
Zhurnal Organicheskoi Khimii 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