Kwiatkowski, Stefan published the artcileReactions of 1,3-dioxacyclanes with acid halides. A new synthesis for ω-halohydrin esters, Synthetic Route of 1193-11-9, the publication is Monatshefte fuer Chemie (1984), 115(6-7), 869-72, database is CAplus.
Dioxolanes I (R = R1 = H, Me, Et; R2 = H, R3 = H, Me, pentyl; R = R2 = R3 = Me, R1 = Ph) reacted with R4CH2COBr (R4 = H, Cl) to give halohydrin esters BrCHR2CHR3O2CCH2R4 in 53-85% yield. Similarly, dioxanes II (R5 = Me, Et) and acyl halides R4CH2COR6 (R4 = H, Cl; R6 = Cl, Br) gave 40-75% R6CH2CH2O2CCH2R4.
Monatshefte fuer Chemie 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