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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649402Generated: October 29, 2026

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

https://huagongshe.com/reaction/649402

Reaction equation

Participants

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

Reaction Steps

In 200 ml of tetrahydrofuran is dissolved 26.8 g of ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)valerate, and 13.4 g of sodium borohydride is added to the solution. Methanol (40 ml) is added dropwise to the mixture at 70° to 80° C. with stirring over the period of 1.5 hours, and after the addition is completed, refluxing is effected for another 2 hours. The reaction solution is concentrated under reduced pressure, and 300 ml of water is added to the residue, followed by extraction with 300 ml of ethyl acetate. The extract is washed with 50 ml of 1N hydrochloric acid and 50 ml of water successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 23 g of 5-(1-benzyloxycarbonyl-4-piperidyl)pentanol as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739066
Source datasetuspto-grants-1988_04
ORD IDord-8541766b75544464ac8980c53dc77714
Source noteuspto-grants-1988_04