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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl-2-(2-ethoxytetrahydrofuran-3-yl)-2-oxoacetateHCID 67607633—
SolventEthanolHCID 702—
ProductHexahydrofuro(2,3-b)furan-3-olHCID 989883293%

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841467B2
Source datasetuspto-grants-2014_09
ORD IDord-ab522e8fb3164449ba295295a0afebbb
Source noteuspto-grants-2014_09