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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476982Generated: October 30, 2026

Triethylamine → N-[(R)-1-ethoxycarbonyl-2-heptylthioethyl]-alanine t-butyl ester

https://huagongshe.com/reaction/476982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl 2-bromopropanoateHCID 545327—
ReactantS-heptyl-L-cysteine ethyl esterHCID 13647885—
SolventHexamethylphosphoramideHCID 12679—
ProductN-[(R)-1-ethoxycarbonyl-2-heptylthioethyl]-alanine t-butyl esterHCID 13647889—

Reaction Steps

In 20 ml of HMPA were dissolved 5.9 g of S-heptyl-L-cysteine ethyl ester and 5.5 g of 2-bromopropionic acid t-butyl ester. A 3.4 ml quantity of triethylamine was added to the solution. The mixture was stirred at room temperature for 24 hours. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate. The extract was sufficiently washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was separated and purified by silica gel column chromatography (a 1:3 mixture of ether and n-hexane as an eluent), producing the α-isomer of the title compound as a colorless oil from the first eluate. Yield 2.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886813
Source datasetuspto-grants-1989_12
ORD IDord-38a6d986becf47b1ae07f3b35b88d9d0
Source noteuspto-grants-1989_12