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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717464Generated: October 31, 2026

Triethylamine → 3-Chloro-5-difluoromethoxy-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/1717464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Chloro-5-(difluoromethoxy)benzoic acidHCID 21904606—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Chloro-5-difluoromethoxy-N-methoxy-N-methylbenzamideHCID 2190465893.8%

Reaction Steps

3-Chloro-5-difluoromethoxybenzoic acid (1.8 g, 8 mmol; see step (iii) above) and oxalyl chloride (1.5 g, 11.8 mmol) were dissolved in methylene chloride (50 mL). DMF (2 drops) was added and the reaction mixture was stirred at ambient temperature for 30 minutes. Then, N,O-dimethylhydroxylamine (1 g, 10.2 mmol) and triethylamine (3 g, 30 mmol) were added and after another 10 minutes stirring at ambient temperature, the reaction mixture was concentrated at reduced pressure. The residue was taken up in ether (100 mL) and water (50 mL). After separation, the organic phase washed with brine, dried over sodium sulphate, filtered and concentrated. This residue was chromatographed on silica (hexane/ethyl acetate 2:1) which gave 2 g, 7.5 mmol (93%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803954B2
Source datasetuspto-grants-2010_09
ORD IDord-9186e66342b04e2a94289a508be26877
Source noteuspto-grants-2010_09