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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394842Generated: October 28, 2026

Pyridine → 3-Thiophenecarboxamide,N-ethyl-

https://huagongshe.com/reaction/2394842

Reaction equation

Participants

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

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811411
Source datasetuspto-grants-1998_09
ORD IDord-6d7e25014e944e73a3dbbf3acc2cc0ea
Source noteuspto-grants-1998_09