HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78753Generated: October 26, 2026
Triethylamine → Hexahydrofuro(2,3-b)furan-3-ol
https://huagongshe.com/reaction/78753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate | HCID 67607633 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Hexahydrofuro(2,3-b)furan-3-ol | HCID 9898832 | 93% |
Reaction Steps
Dissolve sodium borohydride (35.5 g) in ethanol (400 ml) under nitrogen atmosphere. Ethyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetate (100 g) was dissolved in Ethanol (100 ml) and slowly added at 15-30° C. Reaction mass was then maintained at 50-60° C. for 8 hrs. Reaction mass was cooled to 20-30° C. and slowly added ammonium chloride solution (57.5 g in 100 ml water) and stirred for 1 hrs. Reaction mass was filtered and filtrate was distilled out under vacuum to residue. Dichloromethane (400 ml) was added to residue and cooled to −10° C. Hydrochloric acid (85 ml) was added slowly drop wise in 2 hours by maintaining temp 0 to −10° C. Reaction temp was maintained for 1 hr at 0 to −10° C. Triethyl amine (91.3 g) was added to the reaction mass at 0 to −10° C. and reaction mass was stirred for 1 hour at 0 to −10° C. Reaction mass was concentrated to residue. Residue was stripped out with Ethyl acetate (2×100 ml). Ethyl acetate (500 ml) was added to the residue and cooled to 10-15° C. Reaction mass was then filtered off and filtrate was concentrated to residue to get Hexahydrofuro[2,3-b]furan-3-ol (Yield 56 g).
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-ab522e8fb3164449ba295295a0afebbb |
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| Source note | uspto-grants-2014_09 |
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