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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536448Generated: October 30, 2026

Hydrochloric Acid → 1-[2-Hydroxy-4-(trifluoromethyl)phenyl]ethan-1-one

https://huagongshe.com/reaction/536448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Hydroxy-4-(trifluoromethyl)benzoic acidHCID 164578—
ReactantHCID 178418348HCID 178418348—
SolventEthyl AcetateHCID 8857—
Product1-[2-Hydroxy-4-(trifluoromethyl)phenyl]ethan-1-oneHCID 15446449—

Reaction Steps

A solution of 2-hydroxy-4-(trifluoromethyl)benzoic acid (10.0 g, 48.5 mmol) and THF (100 mL) was cooled to <5° C. and methyllithium (95 mL, 1.6M solution in diethyl ether, 152 mmol) was slowly added, keeping the internal temperature <20° C. The resulting solution was warmed to ambient temperature and stirred for 1 hour. The solution was then cooled to 10° C. and treated carefully with EtOAc (100 mL) and 2N HCl (100 mL). The reaction mixture was further diluted with EtOAc (100 mL) then washed with water (100 mL) and brine (20 mL). The organic portion was dried (Na2SO4), filtered, and concentrated to give the title compound (10.3 g). This material was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859584B2
Source datasetuspto-grants-2014_10
ORD IDord-8de4664b1b0e4a0f9b9e167bc9f61ea6
Source noteuspto-grants-2014_10