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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455165Generated: October 30, 2026

Methanol → N-[3-(4-amino-2-cyanophenoxy)phenyl]-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/455165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-[3-(2-cyano-4-nitrophenoxy)phenyl]-2,2,2-trifluoroacetamideHCID 86644681—
CatalystHCID 178418390HCID 178418390—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-[3-(4-amino-2-cyanophenoxy)phenyl]-2,2,2-trifluoroacetamideHCID 8664468297%

Reaction Steps

To a solution of N-[3-(2-cyano-4-nitrophenoxy)phenyl]-2,2,2-trifluoroacetamide (2.81 g, 8.01 mmol) in 1-methylpyrrolidin-2-one (20 mL)/methanol (80 ml) was added 10% palladium-carbon (300 mg), and the mixture was stirred at room temperature for 6 hr under a hydrogen atmosphere (1 atm). Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate (200 ml), washed successively with water (100 mL×2) and saturated brine (100 mL×2), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/n-hexane=50/50→80/20), and the fraction containing the object product was concentrated under reduced pressure to give the title compound (2.48 g, 97%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497274B2
Source datasetuspto-grants-2013_07
ORD IDord-68a4abf4219f4c79b7580e6d758d21ff
Source noteuspto-grants-2013_07