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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079560Generated: October 25, 2026

Hydrochloric Acid → 3-Fluoro-2-methyl-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/2079560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
Reactant3-Fluoro-4-(trifluoromethyl)benzoic acidHCID 688293—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-2-methyl-4-(trifluoromethyl)benzoic acidHCID 57457765—

Reaction Steps

25.0 g (120.1 mmol) of 3-fluoro-4-trifluoromethylbenzoic acid were dissolved in 250 ml of THF, and 100.9 ml (2.5M in hexane, 252.3 mmol) of n-butyllithium were added dropwise at −40° C. The mixture was stirred for 3.5 h, and a solution of 51.2 g (360.4 mmol) of iodomethane in 50 ml of dry THF was then added dropwise. The mixture was stirred for 16 h, and after half an hour the temperature slowly increased to room temperature (RT). For work-up, 150 ml of 1M HCl were added carefully. The mixture was extracted with diethyl ether, and the organic phase was then extracted with 1M NaOH. The aqueous phase was acidified and then extracted with diethyl ether. The organic phase was washed with water, dried and freed from the solvent. The residue was titrated with n-heptane and the solid was removed by filtration. What was isolated were 13.5 g of the pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932211B2
Source datasetuspto-grants-2011_04
ORD IDord-3dd76539f26e43b6beffd9a4265cf53f
Source noteuspto-grants-2011_04