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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768060Generated: October 25, 2026

Triethylamine → 1-Allyloxy-4-chloromethyl-benzene

https://huagongshe.com/reaction/1768060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(4-(Prop-2-en-1-yloxy)phenyl)methanolHCID 11744970—
SolventDichloromethaneHCID 6344—
Product1-Allyloxy-4-chloromethyl-benzeneHCID 12347936—

Reaction Steps

7.67 g (67.0 mmol) methanesulfonyl chloride were given at 0° C. to a solution of 10.0 g (60.9 mmol) (4-allyloxy-phenyl)-methanol and 9.34 ml (67.0 mmol) triethylamine in 35 ml dichloromethane and stirred at r.t. overnight. The mixture was poured in ice water, extracted with dichloromethane and the organic phase dried over Na2SO4. After removal of solvents the residue was purified by chromatography on silica gel (ethyl acetate/n-heptane 1:5) to yield 3.12 g (28%) pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235574B2
Source datasetuspto-grants-2007_06
ORD IDord-a4bb0bfb1f524dbeb1f90661deb84a55
Source noteuspto-grants-2007_06