HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-AMINO-N-THIAZOL-2-YL-BENZAMIDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Nitro-N-(1,3-thiazol-2-yl)benzamide | HCID 230363 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-AMINO-N-THIAZOL-2-YL-BENZAMIDE | HCID 225470 | — |
Reaction Steps
4-Nitro-N-thiazol-2-yl-benzamide (28 mmol) was suspended in abs. EtOH (400 mL) and ethyl acetate (200 mL) and glacial acetic acid (50 mL) was added followed by 10% Pd/C (0.5 g). The mixture was hydrogenated for 72 h at 3 bar H2. The hydrogenation mixture was filtered, and the solvent was removed under reduced pressure. The crude product was added NaHCO3 (sat.) and ethyl acetate, the remaining solid fraction was removed by filtration and dried in vacuo. The liquid phases were separated, the organics were washed with brine, dried over MgSO4, filtered and evaporated to yield a solid. The solid fractions were combined.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674912B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-9a61c3e0078b4a8a971519cfc66ed2a0 |
| Source note | uspto-grants-2010_03 |