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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504829Generated: October 27, 2026

Triethylamine → ethoxycarbonyl N-(tert-butoxycarbonyl)-S-methylcysteinate

https://huagongshe.com/reaction/1504829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantBoc-cys(ME)-OHHCID 7018744—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productethoxycarbonyl N-(tert-butoxycarbonyl)-S-methylcysteinateHCID 86731709—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of N-(tert-butoxycarbonyl)-S-methylcysteine (23.5 g, 0.100 mol) in THF (400 mL) was added dropwise ethylchloroformate (9.6 mL, 0.10 mol) and triethylamine (10.1 g, 0.100 mol) slowly at −10° C. The reaction mixture was stirred at −10° C. for 30 minutes, and then the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to give ethoxycarbonyl N-(tert-butoxycarbonyl)-S-methylcysteinate which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216173B2
Source datasetuspto-grants-2015_12
ORD IDord-7e9000d3f83b43d3a06bff4ccc40ff3c
Source noteuspto-grants-2015_12