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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991147Generated: October 27, 2026

O-Cresol → 2-[4-(Trifluoromethyl)benzyloxy]toluene

https://huagongshe.com/reaction/1991147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-CresolHCID 335—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
SolventDimethylformamideHCID 6228—
Product2-[4-(Trifluoromethyl)benzyloxy]tolueneHCID 1121932197.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Methylphenol (12.53 g, 115.9 mmol) was dissolved in DMF (60 mL), and stirred at 0° C. To the solution was added K2CO3 (24.03 g, 173.9 mmol) and 4-trifluoromethylbenzyl bromide (23.08 g, 96.6 mmol), and the reaction was stirred at room temperature for 2 h. Water was added to the reaction, and the product was extracted with EtOAc twice. The organic layer was washed with water and brine, dried over Na2SO4, and concentrated in vacuo to give a crude residue. The crude residue was purified using silica gel column chromatography (hexane/EtOAc=30/1) to give 4.1 (25.1 g). 1H NMR (400 MHz) (CDCl3) δ 7.64 (2H, d, J=8.2 Hz); 7.56 (2H, d, J=8.2 Hz); 7.18-7.08 (2H, m); 6.90 (1H, t, J=7.2 Hz); 6.84 (1H, d, J=8.1 Hz); 5.14 (2H, s); 2.30 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645779B2
Source datasetuspto-grants-2010_01
ORD IDord-677552d421434f579cd46942fd425de6
Source noteuspto-grants-2010_01