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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7426Generated: October 25, 2026

Triethylamine → 3-Chloro-4-methoxybenzyl chloride

https://huagongshe.com/reaction/7426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(3-Chloro-4-methoxyphenyl)methanolHCID 4312004—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-4-methoxybenzyl chlorideHCID 1115981461.1%

Reaction Steps

To a solution of 3-chloro-4-methoxybenzyl alcohol (1.1 g, 6 mmol) in tetrahydrofuran (5 mL) were added under ice-cooling triethylamine (1.67 mL, 12 mmol) and methanesulfonyl chloride (0.51 ml, 6 mmol) and the mixture was stirred at room temperature for 18 h. The solvent was evaporated under reduced pressure and the obtained residue was dissolved in ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give an almost pure title compound (700 mg, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087597B1
Source datasetuspto-grants-2006_08
ORD IDord-e4e85b88e8b940a682a714ca09b108c4
Source noteuspto-grants-2006_08