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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503113Generated: October 29, 2026

Dimethyl Sulfate → 1-Chloro-2-(methoxymethyl)-4-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1503113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-(trifluoromethyl)benzylalcoholHCID 2778110—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-2-(methoxymethyl)-4-(trifluoromethyl)benzeneHCID 6798274894%

Reaction Steps

A mixture of (2-chloro-5-(trifluoromethyl)phenyl)methanol (COK) (11.55 g, 55 mmol), NaOH (8.00 g, 200 mmol) and dimethyl sulfate (6.25 mL, 65 mmol) in THF (100 mL) was stired for 5 hours at room temperature. The reaction was quenched with water (20 mL) and 25% ammonia (5 mL) and the resulting mixture was stirred overnight at room temperature. The mixture was purred into water (100 mL) and extracted with petroleum ether (100 mL). The organic phase was washed with 1 M NaOH (aq) (100 mL), water (3×100 mL), brine (50 mL), dried over Na2SO4 and filtered. The solvent was removed under reduced pressure to yield 1-chloro-2-(methoxymethyl)-4-(trifluoromethyl)benzene (COMK) as a colorless oil (11.54 g, 94%): 1H NMR (CDCl3) 3.50 (s, 3H), 4.57 (s, 2H), 7.46 (m, 2H), 7.77 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212118B2
Source datasetuspto-grants-2015_12
ORD IDord-3f766ee56a0645d385e1e1099fed2676
Source noteuspto-grants-2015_12