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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100641Generated: October 26, 2026

Oxalyl chloride → Methyl 2-chloro-5-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/2100641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Chloro-5-(trifluoromethyl)benzoic acidHCID 688182—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-chloro-5-(trifluoromethyl)benzoateHCID 15010065100.4%

Reaction Steps

To a solution of 2-chloro-5-(trifluoromethyl)benzoic acid (15 g, 66.8 mmol) in methylene chloride (200 mL) was added oxalyl chloride (12.7 g, 100 mmol) drop wise followed by the addition of 5-6 drops of DMF. The reaction mixture was concentrated, the residue partitioned between methylene chloride and 5% aq. sodium carbonate. The organic layer was dried (MgSO4) and concentrated to give the title compound as a pale oil (16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572805B2
Source datasetuspto-grants-2009_08
ORD IDord-bea4f7d9b8614ef2b3354384d0dc7cad
Source noteuspto-grants-2009_08