Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485184Generated: October 30, 2026

Triethylamine → HCID 131713673, compound

https://huagongshe.com/reaction/485184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 131713674HCID 131713674—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131713673HCID 131713673—

Reaction Steps

A mixture of L-alanyl-L-proline, phenylmethyl ester, p-toluenesulfonic acid salt (32.16 g., 72 mmole), tert-butyl bromoacetate (14.2 g., 72 mmole), triethylamine (20.1 ml., 144 mmole), and tetrahydrofuran (290 ml.) are stirred at room temperature for 72 hours. Benzyl chloroformate (12.4 ml., 87.8 mmole) and triethylamine (12.5 ml., 87.8 mmole) are added and the mixture stirred overnight. The reaction product is evaporated, and partitioned between water and ethyl acetate. The ethyl acetate solubles are washed with dilute hydrochloric acid and then water. The ethyl acetate solution is then evaporated and chromatographed over silica gel (mesh 230-400) using the solvent system ethyl acetate/hexane (1:1) (10 psi pressure) to give 19.5 g. of 1-[N-[2-(1,1-dimethylethylethoxy)-2-oxoethyl]-N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-proline, phenylmethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535176
Source datasetuspto-grants-1985_08
ORD IDord-72dbb33b19e2491d830aeafd38e15063
Source noteuspto-grants-1985_08