HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-Thiophenecarboxamide,N-ethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thiophene-3-carboxylic acid | HCID 6918 | — |
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Thiophenecarboxamide,N-ethyl- | HCID 15452328 | 76% |
Reaction Steps
A mixture of thiophene-3-carboxylic acid (20.0 g, 178 mmol), thionyl chloride (30 mL, 411 mmol), and catalytic DMF (5 drops) was stirred at RT overnight. This solution was concentrated under vacuum, and stripped several times from toluene to remove all traces of excess thionyl chloride. Ethyl amine hydrochloride (29.03 g, 356 mmol) was then added to a solution of this crude acid chloride dissolved in CH2Cl2 (50 mL). Pyridine (31.64 g, 400 mmol) was added, and after 1 h of stirring the reaction was washed with 10% HCl followed with water, dried (MgSO4), concentrated, and recrystallized from EtOAc/hexanes to give 14.9 g of N-ethyl-3-thiophenecarboxamide as a tan solid, a 76% yield. m.p. 115°-117° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811411 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-6d7e25014e944e73a3dbbf3acc2cc0ea |
| Source note | uspto-grants-1998_09 |