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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78754Generated: October 26, 2026

Acetic Anhydride → Hexahydrofuro[2,3-b]furan-3-yl acetate

https://huagongshe.com/reaction/78754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHexahydrofuro(2,3-b)furan-3-olHCID 9898832—
SolventDichloromethaneHCID 6344—
ProductHexahydrofuro[2,3-b]furan-3-yl acetateHCID 2186902287.7%

Reaction Conditions

Temperature5 °C

Reaction Steps

Hexahydrofuro[2,3-b]furan-3-ol (25 g) was dissolved in dichloromethane (250 ml) and added triethylamine (23.3 g). N,N-dimethylaminopyridine (0.46 g) was added to the reaction mass. Reaction mass was cooled to 0-10° C. Acetic anhydride (21.5 g) was diluted with dichloromethane (50 ml) & added slowly drop-wise to the reaction mass. Reaction mass was stirred at 0-5° C. till completion. Reaction mass was washed with water (2×100 ml) & 10% Sodium chloride solution (100 ml). Reaction mass was concentrated under vacuum at <40° C. to get residue of Hexahydrofuro[2,3-b]furan-3-yl acetate (yield 29 g). Further, the product was purified by distillation (20 g) under vacuum using fractional distillation at 88-102° C. to get main fraction 17 g having purity 92.6%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841467B2
Source datasetuspto-grants-2014_09
ORD IDord-a7dd7ca8078f4adcb4feb2a925d82b30
Source noteuspto-grants-2014_09