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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383231Generated: October 30, 2026

Water → N-Methoxy-N-methyl-4-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1383231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventDichloromethaneHCID 6344—
ProductN-Methoxy-N-methyl-4-(trifluoromethyl)benzamideHCID 1406934898.5%

Reaction Steps

To a stirred suspension of 19.9 grams (0.204 mole) of N-methoxy-N-methylamine hydrochloride in 500 mL of methylene chloride was added 39.3 grams (0.388 mole) of triethylamine. Upon completion of addition, the reaction mixture was stirred for ten minutes, and a solution of 38.4 grams (0.185 mole) of 4-trifluoromethylbenzoyl chloride in 25 mL of methylene chloride was added dropwise. Upon completion of addition, the reaction mixture was stirred at ambient temperature for 18 hours. The reaction mixture was then stirred vigorously with 300 mL of water. The aqueous layer was separated from the organic layer and washed with three portions of methylene chloride. The washes were combined with the organic layer, and the combination was dried with magnesium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure, yielding 42.5 grams of N-methoxy-N-methyl-4-trifluoromethylbenzamide as an oil. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808762
Source datasetuspto-grants-1989_02
ORD IDord-ade1b51caa6b467c856872ddd48c8f5c
Source noteuspto-grants-1989_02