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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710107Generated: October 29, 2026

Dimethylformamide → 4-(Trifluoromethyl)benzoyl chloride

https://huagongshe.com/reaction/710107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
ReactantOxalyl chlorideHCID 65578—
SolventDichloromethaneHCID 6344—
Product4-(Trifluoromethyl)benzoyl chlorideHCID 67607—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(Trifluoromethyl)benzoic acid (0.8 g, 4.2 mmol) dissolved in DCM (20 ml), cooled to 0° C. and added oxalyl chloride (0.8 g, 6.1 mmol). Catalytic amount of DMF was added to this mixture and stirred at rt for 30 mins. After 30 mins, DCM removed on rotavapour and co-distilled the residue two times with DCM to obtain 4-(trifluoromethyl)benzoyl chloride quantitatively. 2-Amino-5-bromophenol (0.71 g, 3.8 mmol) dissolved in DCM (20 ml) and added Pyridine (0.32 ml, 4.1 mmol) under nitrogen atmosphere. This mixture stirred at rt for 30 mins and added 4-(trifluoromethyl)benzoyl chloride (0.88 g, 4.2 mmol). After continuing stirring at rt for 15 mins, reaction mass diluted with water and extracted with DCM. DCM layer washed with aq. NaHCO3 and DCM removed on rotavapour to obtain the solid. Solid was triturated with Et2O and Petether mixture (4:1) to obtain the titled compound (0.6 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181214B2
Source datasetuspto-grants-2015_11
ORD IDord-0aa8c96671b840b4a84dcefe1d9c46e8
Source noteuspto-grants-2015_11