HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 1-Tert-butyl-2-methoxy-5-(trifluoromethyl)-4-aminobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-Tert-butyl-2-methoxy-5-(trifluoromethyl)-4-nitrobenzene | HCID 57470246 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Tert-butyl-2-methoxy-5-(trifluoromethyl)-4-aminobenzene | HCID 57470247 | 95.9% |
Reaction Steps
To a refluxing solution of 1-tert-butyl-2-methoxy-5-(trifluoromethyl)-4-nitrobenzene (473 mg, 1.7 mmol) and ammonium formate (473 mg, 7.3 mmol) in EtOH (10 mL) was added 10% Pd—C (200 mg). The mixture was refluxed for 1 h, cooled and filtered through Celite. The solvent was removed by evaporation to give 1-tert-butyl-2-methoxy-5-(trifluoromethyl)-4-aminobenzene (C-18) (403 mg, 95%). 1H NMR (400 MHz, CDCl3) δ 7.19 (s, 1H), 6.14 (s, 1H), 4.02 (bs, 2H), 3.74 (s, 3H), 1.24 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829204B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7e6ec5ffb7444452a365658ce55d9d8d |
| Source note | uspto-grants-2014_09 |