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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexahydrofuro(2,3-b)furan-3-ol | HCID 9898832 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Hexahydrofuro[2,3-b]furan-3-yl acetate | HCID 21869022 | 87.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841467B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a7dd7ca8078f4adcb4feb2a925d82b30 |
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| Source note | uspto-grants-2014_09 |
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