HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Methyl 3-((ethoxycarbonyl)amino)thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-amino-2-thiophenecarboxylate | HCID 89652 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl 3-((ethoxycarbonyl)amino)thiophene-2-carboxylate | HCID 840181 | 98.4% |
Reaction Steps
To a solution of 3-amino-thiophene-2-carboxylic acid methyl ester (2.39 g, 15.2 mmol) in benzene (51 mL) was added K2CO3 (6.30 g, 45.6 mmol) followed by ethyl chloroformate (1.74 mL, 18.2 mmol). After heating at reflux for 12 h, the mixture was filtered and the filtrate was concentrated to afford the desired product (3.43 g), which was used in the next step without further purification. MS: 230.0. 1H NMR (400 MHz, CD3OD) δ ppm 7.82 (d, J=5.5 Hz, 1H), 7.66 (d, J=5.6 Hz, 1H), 4.23 (q, J=7.1 Hz, 2H), 3.86 (s, 3H), 1.32 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193178B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-2c01ccd83eff4bcabc75c1757047dc50 |
| Source note | uspto-grants-2012_06 |