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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604709Generated: October 26, 2026

Dimethylformamide → 5-Bromo-2-chloro-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/604709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
ReactantN,O-dimethoxyhydroxylamine hydrochlorideHCID 22015712—
CatalystOxalyl chlorideHCID 65578—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product5-Bromo-2-chloro-N-methoxy-N-methylbenzamideHCID 5341837999.7%

Reaction Steps

Oxalyl chloride (3.78 mL, 0.0441 mmol) and N,N-dimethylformamide (0.06 mL) were added to a chloroform (20 mL) solution of 5-bromo-2-chlorobenzoic acid (10.0 g, 0.0425 mol). After the reaction mixture was stirred at room temperature for one day, the reaction mixture was evaporated under reduced pressure. The obtained yellow oily substance was dissolved in chloroform (20 mL). This solution was added dropwise to a mixture of N,O-dimethoxyhydroxylamine hydrochloride (4.56 g, 0.0468 mol), triethylamine (12.3 mL, 0.0882 mol) and chloroform (50 mL) for 15 minutes, while maintaining the reaction temperature at 5° C. to 10° C. After stirred for 15 minutes, the reaction mixture was warmed to room temperature. After water (20 mL) was added to the reaction mixture, the organic layer was separated and the organic layer was washed with a saturated sodium bicarbonate aqueous solution and brine, and then dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the solvent was evaporated under reduced pressure to obtain 5-bromo-2-chloro-N-methoxy-N-methylbenzamide (11.8 g, 99.7%) as a colorless crystal. This was used in the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910619B2
Source datasetuspto-grants-2011_03
ORD IDord-c8222074f938427091150ae6ab68adf9
Source noteuspto-grants-2011_03