HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 5-cyano-2-(trifluoromethyl)benzoate → 5-(Aminomethyl)-2-(trifluoromethyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 5-cyano-2-(trifluoromethyl)benzoate | HCID 67970345 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(Aminomethyl)-2-(trifluoromethyl)benzoic acid | HCID 67970667 | 50% |
Reaction Steps
Combine benzyl 5-cyano-2-(trifluoromethyl)benzoate (3.9 g, 12.78 mmol, 1.0 equiv), palladium (10 wt % on carbon, 400 mg, 0.38 mmol, 0.03 equiv), and methanol (128 mL), and purge the mixture with hydrogen. Stir overnight under a hydrogen atmosphere. Filter the mixture through a pad of diatomaceous earth, and then rinse the pad with hot methanol (3×150 mL) to bring through precipitated product. Concentrate the filtrate under reduced pressure to give the title compound (1.4 g, 50%). MS (m/z) 220 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252831B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-21675f574bca4d0eadccd8c716c51bfa |
| Source note | uspto-grants-2012_08 |