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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | N-[3-(2-cyano-4-nitrophenoxy)phenyl]-2,2,2-trifluoroacetamide | HCID 86644681 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-[3-(4-amino-2-cyanophenoxy)phenyl]-2,2,2-trifluoroacetamide | HCID 86644682 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497274B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-68a4abf4219f4c79b7580e6d758d21ff |
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| Source note | uspto-grants-2013_07 |
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