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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980604Generated: October 29, 2026

Acetic Acid → Ethyl 4-(1-benzyloxycarbonyl-4-piperidyl)-2-hydroxybutyrate

https://huagongshe.com/reaction/980604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 4-(1-benzyloxycarbonyl-4-piperidyl)-2-oxobutyrateHCID 19868897—
SolventEthanolHCID 702—
ProductEthyl 4-(1-benzyloxycarbonyl-4-piperidyl)-2-hydroxybutyrateHCID 2014371867.3%

Reaction Steps

In 30 ml of ethanol is dissolved 17 g of ethyl 4-(1-benzyloxycarbonyl-4-piperidyl)-2-oxobutyrate, and 4.5 g of acetic acid is added to the solution. Sodium cyanoborohydride (3 g) is added to the mixture at room temperature with stirring, followed by stirring at room temperature for 3 hours, and 500 ml of water is added to the reaction mixture, which is extracted with methylene chloride. The extract is dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the resulting residue is purified by silica-gel column chromatography (hexane:ethyl acetate=2:1 to 1:1) to give 11.5 g of ethyl 4-(1-benzyloxycarbonyl-4-piperidyl)-2-hydroxybutyrate as a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04638000
Source datasetuspto-grants-1987_01
ORD IDord-dda132f23b6c484499db454e585b69f6
Source noteuspto-grants-1987_01