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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445295Generated: October 30, 2026

4-(Trifluoromethyl)benzoyl chloride → HCID 9051890, compound

https://huagongshe.com/reaction/445295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Fluorophenyl)ethanamineHCID 533928—
SolventDichloromethaneHCID 6344—
ProductHCID 9051890HCID 9051890—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 250-mL, round-bottomed flask containing a solution of 2-(3-fluorophenyl)ethanamine (1.3 mL, 9.6 mmol) and diisopropylethylamine (1.7 mL, 9.6 mmol) in dichloromethane (32 mL) was cooled to 0° C. and treated dropwise with 4-(trifluoromethyl)benzoyl chloride (2.0 mL, 9.6 mmol) over 5 min. The ice-bath was removed after 2 h and the reaction mixture was stirred overnight. The precipitate formed was collected by filtration. The filtrate was diluted with dichloromethane (100 mL) and transferred to a separatory funnel and extracted with water (35 mL). The dichloromethane layer was separated and formation of precipitate was observed which was collected by filtration. The filtrate was concentrated to yield more solid and the combined solids were dried under vacuum to yield N-(3-fluorophenethyl)-4-(trifluoromethyl)benzamide as a white solid. MS (ESI pos. ion) m/z: 312 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476297B2
Source datasetuspto-grants-2013_07
ORD IDord-610b75128ad947a3b3d632a90f6cb371
Source noteuspto-grants-2013_07