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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194970Generated: November 1, 2026

Oxalate → HCID 9983610, compound

https://huagongshe.com/reaction/1194970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalateHCID 71081—
ReactantL-Alanine 1,1-dimethylethyl esterHCID 89016—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-oxohexanoateHCID 13817563—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 9983610HCID 998361011.5%

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 numberUS04816466
Source datasetuspto-grants-1989_03
ORD IDord-c2ef57ca6b304b38a1ca91723e3158d4
Source noteuspto-grants-1989_03