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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376811Generated: October 26, 2026

Triethylamine → N-Bromoacetyl-S-triphenylmethyl-L-cysteine ethyl ester

https://huagongshe.com/reaction/376811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
ReactantS-trityl-cysteine ethyl esterHCID 21144450—
SolventTetrahydrofuranHCID 8028—
ProductN-Bromoacetyl-S-triphenylmethyl-L-cysteine ethyl esterHCID 5731872669%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of S-triphenylmethyl-L-cysteine ethyl ester (18 g, 46 mmol.) and triethylamine (6.4 mL, 46 mmol.) in dry THF (250 mL) under nitrogen was cooled to 0° C. A solution of bromoacetyl bromide (9.28 g, 46 mmol.) in dry THF (60 mL) was added dropwise during which time the solution turned cloudy. The reaction mixture was stirred at 0° C. for 1 h and then at room temperature for 1 h. The reaction mixture was filtered and the filtrate was concentrated in vacuo to give an oil. The oil was partitioned between methylene chloride and water (60 mL each), the organic layer washed with 5% HCl, NaHCO3, dried (magnesium sulfate), filtered, and the volatiles removed to give the desired product (69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022523
Source datasetuspto-grants-2000_02
ORD IDord-99e1d454d0384ee4a57b68b1ad558de0
Source noteuspto-grants-2000_02