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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010822Generated: October 25, 2026

2-Fluorobenzoyl chloride → 2-(2-Fluorobenzamido)thiophene-3-carboxamide

https://huagongshe.com/reaction/1010822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoyl chlorideHCID 9808—
Reactant2-Aminothiophene-3-carboxamideHCID 699495—
SolventPyridineHCID 1049—
Product2-(2-Fluorobenzamido)thiophene-3-carboxamideHCID 716410277%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-thiophene-3-carboxylic acid amide (8.73 g, 61.4 mmole) was dissolved in pyridine (100 ml), cooled to 0° C., and 2-fluorobenzoyl chloride was added dropwise over 20 min, then the reaction was allowed to warm to room temperature with stirring overnight. The pyridine was removed under vacuum, dichloromethane and water were added. The product was precipitated as a grey solid and was washed with diluted hydrochloric acid, water and air dried. The dichloromethane layer was separated, washed with diluted hydrochloric acid, and water, dried over sodium sulfate (anh.) and the solvent was removed to give a total of 12.45 g product (77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977342B2
Source datasetuspto-grants-2011_07
ORD IDord-863d6cffb27e476494e14d237ff3589b
Source noteuspto-grants-2011_07