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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267475Generated: October 30, 2026

Benzoyl chloride → N-(2-(thiophen-3-yl)ethyl)benzamide

https://huagongshe.com/reaction/2267475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-(Thiophen-3-yl)ethan-1-amine hydrochlorideHCID 12258738—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-(thiophen-3-yl)ethyl)benzamideHCID 2585416096.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(Thiophen-3-yl)ethanamine hydrochloride (3 g, 18 mmol) was taken in THF (40 mL) and treated with triethylamine (9.92 mL, 71.2 mmol). The reaction was cooled down to 0° C. and benzoyl chloride (2.55 mL, 21.9 mmol), diluted with THF was added dropwise to the reaction. The reaction was stirred for 3 h and the volatiles removed in vacuo. The residue was dissolved in ethyl acetate and washed with an aqueous saturated solution of sodium bicarbonate, water and brine. The organic solution was dried with sodium sulfate and purified by flash chromatography using a gradient of 25 to 70% ethyl acetate in hexanes to afford an off-white solid (4 g). MS (M+H)+ 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-b24ff8e5f98c48cf80f6b18c53d4186a
Source noteuspto-grants-2010_12