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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440570Generated: November 1, 2026

Pyridine → 3-Thiophenecarboxamide,N-ethyl-

https://huagongshe.com/reaction/1440570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThiophene-3-carboxylic acidHCID 6918—
ReactantEthylamine hydrochlorideHCID 11198—
ReactantThionyl ChlorideHCID 24386—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product3-Thiophenecarboxamide,N-ethyl-HCID 1545232876%

Reaction Steps

A mixture of 3-thiophenecarboxylic acid (20 g, 178 mmol), thionyl chloride (30 mL), and DMF (5 drops) was stirred overnight, then was concentrated under vacuum and stripped several times from toluene to remove all traces of excess thionyl chloride. Pyridine (31.64 g, 400 mmol) was added dropwise to a mixture of this acid chloride and ethylamine hydrochloride in toluene (5 mL) and CH2Cl2 (50 mL). After stirring for 1 h, the reaction was washed with 10% aq HCl followed with water, then was dried (MgSO4), concentrated, and crystallized from ethyl acetate/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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498630
Source datasetuspto-grants-1996_03
ORD IDord-c8a333a8a8194d1d9d940d689aef5b0d
Source noteuspto-grants-1996_03