Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697208Generated: October 31, 2026

1-Chloro-1-(4-methoxyphenyl)-1-trifluoromethylethane → 1-Methoxy-4-(1,1,1-trifluoro-2-methylpropan-2-yl)benzene

https://huagongshe.com/reaction/1697208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-1-(4-methoxyphenyl)-1-trifluoromethylethaneHCID 13885600—
ReactantTrimethylaluminumHCID 16682925—
SolventHydrochloric AcidHCID 313—
Product1-Methoxy-4-(1,1,1-trifluoro-2-methylpropan-2-yl)benzeneHCID 18333624—

Reaction Conditions

Temperature95 °C

Reaction Steps

A solution of 1-(2-chloro-1,1,1-trifluoropropan-2-yl)-4-methoxybenzene (18.0 g, 75 mmol) in 400 ml of hexanes was treated with trimethylaluminum (151 ml, 302 mmol) (2.0 M in heptane) at rt and the resulting mixture was heated at 95° C. overnight. The reaction mixture was cooled in an ice-water bath, conc. HCl was added to the reaction mixture dropwise. Fumes were generated. After about 10 ml of conc. HCl was added, more rapid addition of acid was possible due to the near complete quenching of the unreacted AlMe3. After addition of 100 ml of conc. HCl, 250 ml of H2O was added and the mixture was stirred vigorously for 1 h. The layers were separated. The org layer was dried (Na2SO4) and concentrated to give the title compound as an oil, which solidified upon drying on the vac line.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163909B2
Source datasetuspto-grants-2012_04
ORD IDord-73539ae066094bd58ac03e111284f719
Source noteuspto-grants-2012_04