HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 5-(3-Amino-2-methoxy-5-methyl-phenyl)-thiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 5-(3-Nitro-2-methoxy-5-methyl-phenyl)thiophene-2-carboxylic acid | HCID 57483819 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(3-Amino-2-methoxy-5-methyl-phenyl)-thiophene-2-carboxylic acid | HCID 57483820 | 99% |
Reaction Steps
5-(3-Nitro-2-methoxy-5-methyl-phenyl)thiophene-2-carboxylic acid 24b (0.29 g, 1 mmol) was dissolved in 30 mL of ethyl acetate followed by addition of 0.06 g of palladium on carbon and ammonium formate (0.25 g, 4 mmol). Upon completion of the addition, the reaction mixture was heated to reflux for 45 minutes. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered to remove palladium on carbon. The filtrate was concentrated under reduced pressure and dried to obtain the title compound 5-(3-amino-2-methoxy-5-methyl-phenyl)-thiophene-2-carboxylic acid 24c (0.26 g, yield 99%) as a green solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367710B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-a254bd0597f545d9b97182b93769115d |
| Source note | uspto-grants-2013_02 |