Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869937Generated: October 31, 2026

Oxalyl chloride → 3-bromo-N-cyclopropyl-4-methylbenzamide

https://huagongshe.com/reaction/1869937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantCyclopropylamineHCID 69828—
Reactant3-Bromo-4-methylbenzoic acidHCID 82130—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-bromo-N-cyclopropyl-4-methylbenzamideHCID 21107152—

Reaction Steps

A stirred, cooled (ice bath) solution of 3-bromo-4-methyl-benzoic acid (Aldrich, 5 g, 23.25 mmol) in benzene (50 mL), dichloromethane (10 mL) and N,N-dimethylformamide (0.5 mL) was treated with oxalyl chloride (4 mL, 46.5 mmol). The reaction mixture was allowed to warm to ambient temperature over 3 h. The volatiles were then distilled off in vacuo, the residue was diluted with anhydrous dichloromethane (50 mL) under argon, cooled (ice bath) and treated with 4-(dimethylamino)pyridine (5.67 g, 46.5 mmol) followed by cyclopropyl amine (1.93 mL, 27.9 mmol). After 3 h, the reaction mixture was diluted with dichloromethane and washed with water. The organic phase was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford the title product that was used as such for the next step (6.0 g, ˜100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638648B2
Source datasetuspto-grants-2009_12
ORD IDord-43650ba22a6449409b0d8cb8c0237e1e
Source noteuspto-grants-2009_12