HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzofurancarboxylic acid, 5-nitro-, ethyl ester → Ethyl 5-aminobenzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzofurancarboxylic acid, 5-nitro-, ethyl ester | HCID 1382954 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-aminobenzofuran-2-carboxylate | HCID 9837138 | — |
Reaction Steps
Ethyl 5-nitrobenzofuran-2-carboxylate (Aldrich, 8.0 g) was dissolved in a mixture of EtOH and THF, treated with 10% Pd/C (wet, Degussa type E101, Aldrich) and hydrogenated on a Parr apparatus at 35 psi for 4 h. The reaction mixture was filtered over Celite, washed with THF and EtOH and concentrated under vacuum to give crude solid product, 6.3 g which was used without purification. 1H NMR (CDCl3) 7.34-7.37 (m, 2H), 6.87 (d, 1H), 6.81 (dd, 1H), 4.41 (q, 2H, OCH2), 3.60 (broad s, 2H, NH2), 1.40 (t, 3H, OCH2CH3); m/z 206.39 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409884B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-b8502854bb9f4cec8001f92442430486 |
| Source note | uspto-grants-2016_08 |