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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978429Generated: October 26, 2026

Benzyl N-(4-aminobutyl)carbamate → Ethyl 2-(4-benzyloxycarbonylaminobutyl)aminomethyl-4-phenylbutyrate

https://huagongshe.com/reaction/978429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl N-(4-aminobutyl)carbamateHCID 2783677—
ReactantEthyl alpha-(phenethyl)acrylateHCID 11117162—
SolventEthanolHCID 702—
ProductEthyl 2-(4-benzyloxycarbonylaminobutyl)aminomethyl-4-phenylbutyrateHCID 20203289—

Reaction Steps

A mixture of 20 g of 4-benzyloxycarbonylamino-1-butylamine, 21.04 g of ethyl α-(phenethyl)acrylate and 200 ml of ethanol was stirred at room temperature for 8 days and evaporated to dryness. The residue was dissolved in ethyl ether and the solution was extracted three times with 100 ml of 2N hydrochloric acid. The aqueous layer was basified with 2N sodium hydroxide and extracted three times with methylene chloride, dried over magnesium sulfate and evaporated to give the ethyl 2-(4-benzyloxycarbonylaminobutyl)aminomethyl-4-phenylbutyrate having signals in the NMR spectrum at δ=7.4, 7.25, and 5.1 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665087
Source datasetuspto-grants-1987_05
ORD IDord-9c2338b2512946f8b623353ee77a3dfe
Source noteuspto-grants-1987_05