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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378003Generated: October 30, 2026

Pyridine → 3-Thiophenecarboxamide,N-ethyl-

https://huagongshe.com/reaction/378003

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 numberUS06028101
Source datasetuspto-grants-2000_02
ORD IDord-3813552462064bf49678fa6cb1f08462
Source noteuspto-grants-2000_02