HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 4-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 4-(3-Nitro-2-methoxy-phenyl)-furan-2-carboxylic acid | HCID 57483824 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acid | HCID 57483825 | 73.4% |
Reaction Steps
4-(3-nitro-2-methoxy-phenyl)-furan-2-carboxylic acid 28c (500 mg, 1.9 mmol) was dissolved in 15 mL of ethyl acetate followed by addition of 100 mg of palladium on carbon and ammonium formate (429 mg, 7.6 mmol). The reaction mixture was heated to reflux for 3 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered to remove palladium on carbon and concentrated under reduced pressure to obtain the title compound 4-(3-amino-2-methoxy-phenyl)-furan-2-carboxylic acid 28d (325 mg, yield 73.4%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367710B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-1bd107c68a4f4c879c7aa67ce1039b8f |
| Source note | uspto-grants-2013_02 |