HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-nitro-1-benzothiophene-2-carboxylate → Ethyl 5-amino-1-benzothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-nitro-1-benzothiophene-2-carboxylate | HCID 737499 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-amino-1-benzothiophene-2-carboxylate | HCID 2764450 | — |
Reaction Steps
A suspension of 5-nitro-benzo[b]thiophene-2-carboxylic acid ethyl ester (10.52 g, 41.89 mmol) and 10% Pd/C (1.1 g) in 450 mL of EtOH was hydrogenated under 1 atm of H2 for 4 d at rt. The reaction mixture was filtered and the filtrate was concentrated and dried to give 5-amino-benzo[b]thiophene-2-carboxylic acid ethyl ester as a green solid. A parallel reaction was preformed on 10.61 g of 5-nitro-benzo[b]thiophene-2-carboxylic acid ethyl ester in the same manner. A total of 18.37 g of 5-amino-benzo[b]thiophene-2-carboxylic acid ethyl ester was obtained. MS (EI): cal'd 222.0 (MH+), exp 222.2 (MH+). Procedure for Acylation
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872024B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-305413ff6bf14c38a2a1d4db9d30a2bf |
| Source note | uspto-grants-2011_01 |