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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351220Generated: November 2, 2026

Sodium Acetate → HCID 9983610, compound

https://huagongshe.com/reaction/2351220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-oxohexanoateHCID 13817563—
ReactantHCID 86743427HCID 86743427—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 9983610HCID 998361015.7%

Reaction Steps

A mixture of 5 g of L-alanine tert-butyl ester·oxalate, 11 g of ethyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-oxohexanoate, 1.6 g of sodium acetate, 1.2 g of acetic acid and 100 ml of ethanol is stirred at room temperature for 1 hour, and a solution of 1.9 g of sodium cyanoborohydride in 100 ml of ethanol is added dropwise to the mixture over a period of 4 hours. After stirring at room temperature overnight, 500 ml of water is added to the reaction mixture, and the mixture is extracted with 300 ml of ethyl acetate. The extract is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue is separated and purified by silica gel column chromatography (hexane:acetone=4:1), whereby the first fraction yields 1.7 g of N-[(R)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl]-L-alanine tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871842
Source datasetuspto-grants-1989_10
ORD IDord-b2cc2469394e41ca8b3df403da02e4bd
Source noteuspto-grants-1989_10