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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710871Generated: October 31, 2026

Diethyl Pyrocarbonate → 3-cyano-N-methoxy-N-methyl-5-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1710871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Cyano-5-(trifluoromethyl)benzoic acidHCID 58902287—
SolventTetrahydrofuranHCID 8028—
Product3-cyano-N-methoxy-N-methyl-5-(trifluoromethyl)benzamideHCID 8662843382%

Reaction Steps

A solution of 3-cyano-5-(trifluoromethyl)benzoic acid (200 mg, 0.93 mmol) in tetrahydrofuran (2 mL) was added with N,O-dimethylhydroxyamine hydrochloride (145 mg, 1.49 mmol), N,N-diisopropylethylamine (470 mg, 3.64 mmol) and DEPC (227 mg, 1.39 mmol) with stirring on an ice bath, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, the resulting residue was added with 1 M hydrochloric acid (0.5 mL), and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain 3-cyano-N-methoxy-N-methyl-5-(trifluoromethyl)benzamide (196 mg, 82%) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790737B2
Source datasetuspto-grants-2010_09
ORD IDord-aa885f945ef445519ec5d7c27a73c361
Source noteuspto-grants-2010_09