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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913284Generated: November 1, 2026

Methane → 1-(2-Hydroxy-4-(trifluoromethyl)phenyl)ethan-1-one

https://huagongshe.com/reaction/1913284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
Reactant2-Hydroxy-4-(trifluoromethyl)benzoic acidHCID 164578—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
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. (internal temperature) and methyllithium (95 mL of a 1.6M solution in Et2O, 152 mmol) was added, keeping the internal temperature ≦20° C. (slow addition, methane generation). Following methyllithium addition, the solution was warmed to ambient temperature and stirred for 1 h. The solution was then re-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 1-(2-hydroxy-4-(trifluoromethyl)phenyl)ethanone (10.3 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609692B2
Source datasetuspto-grants-2013_12
ORD IDord-ecf0130c51da4f0eb432a3327d5c8460
Source noteuspto-grants-2013_12