HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 4-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4-(3-Nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid | HCID 57483844 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid | HCID 57483845 | 113.4% |
Reaction Steps
4-(3-Nitro-2-methoxy-phenyl)-thiophene-2-carboxylic acid 19a (400 mg, 1.45 mmol) was dissolved in 30 mL of ethyl acetate followed by addition of 100 mg of palladium on carbon (10%) and ammonium formate (360 mg, 5.8 mmol). The mixture was heated to reflux for 3 hours. The mixture was filtered and concentrated under reduced pressure to obtain the title compound 4-(3-amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid 19b (410 mg) as a brown oil, which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642637B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-5d16b0e5c606447481e7a34422ed1791 |
| Source note | uspto-grants-2014_02 |