Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121203Generated: November 2, 2026

Oxalyl chloride → (4-Bromomethyl-2-phenylbenzoyl)methionine methyl ester

https://huagongshe.com/reaction/2121203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
Reactant4-Bromomethyl-2-phenylbenzoic acidHCID 23436455—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product(4-Bromomethyl-2-phenylbenzoyl)methionine methyl esterHCID 5432373875%

Reaction Steps

To a solution in dichloromethane (25 mL) of 4-bromomethyl-2-phenylbenzoic acid (2.16 g, 7.42 mmol), prepared as in Example 234B, was added oxalyl chloride (0.84 mL, 965 mmol) and 2 drops on DMF and the reaction mixture was stirred for 2 hours. The reaction mixture was concentrated in vacuo and azeotroped with toluene. The residue was dissolved in dichloromethane (15 mL) and then was added to a solution in dichloromethane (15 mL) of methionine methyl ester hydrochloride (1.78 g, 8.90 mmol) and diisopropylethylamine (3.10 g, 17.81 mmol) (prepared at −10° C.) dropwise. The reaction mixture was stirred for 30 minutes and then was poured into ether and extracted with water, aqueous 3N HCl (2×) and brine, dried, filtered and concentrated in vacuo. Chromatography on silica gel (5% ethyl acetate-chloroforn) to give (4-bromomethyl-2-phenylbenzoyl)methionine methyl ester (2.42 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693123B2
Source datasetuspto-grants-2004_02
ORD IDord-6535fdc3bacd48aea04de25869f6359c
Source noteuspto-grants-2004_02