HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester → 4-(5-Amino-thiophen-2-yl)-butyric acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester | HCID 69233400 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(5-Amino-thiophen-2-yl)-butyric acid methyl ester | HCID 69235562 | 66.2% |
Reaction Steps
A mixture of 4-(5-nitro-thiophen-2-yl)-butyric acid methyl ester (2.29 g, 10.0 mmol) and palladium hydroxide (500 mg, 20% on carbon) in 30 mL of ethyl acetate and 30 mL of methanol is hydrogenated at 50 psi for 48 hours. The reaction mixture is filtered and concentrated. The residue is purified by flash column chromatography eluting with 1:3 ethyl acetate:hexane to provide 1.32 g of 4-(5-amino-thiophen-2-yl)-butyric acid methyl ester as a dark oil; 1H NMR (DMSO-d6) δ 1.74 (m, 2H), 2.38 (m, 2H), 2.54 (m, 2H), 3.59 (s, 3H), 5.66 (d, J=3 Hz, 1H), 6.24 (d, J=3 Hz, 1H); MS 200.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06987116B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-93728a921a6f4cff8cd5aac40a9f16f2 |
| Source note | uspto-grants-2006_01 |