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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464889Generated: October 29, 2026

Tetrahydrofuran → 5-(1-Benzyloxycarbonyl-4-piperidyl)pentanol

https://huagongshe.com/reaction/464889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-(1-benzyloxycarbonyl-4-piperidyl)valerateHCID 14046929—
SolventMethanolHCID 887—
Product5-(1-Benzyloxycarbonyl-4-piperidyl)pentanolHCID 1404693097.6%

Reaction Steps

To a stirred mixture of ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)valerate (26.8 g), tetrahydrofuran (200 ml) and sodium borohydride (13.4 g) is added dropwise methanol (40 ml) for 1.5 hours at 70°-80° C. After the addition is complete, the mixture is refluxed for 2 hours with stirring. After evaporation of solvent, the residue is diluted with water (300 ml) and extracted with ethyl acetate (300 ml). The extract is washed successively with 1N hydrochloric acid and water, dried over anhydrous magnesium sulfate and evaporated in vacuo to give 5-(1-benzyloxycarbonyl-4-piperidyl)pentanol (23 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548932
Source datasetuspto-grants-1985_10
ORD IDord-96b520d745e94115aff2239902f52f9a
Source noteuspto-grants-1985_10