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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15252Generated: October 31, 2026

Dichloromethane → 3,5-Bis(chloromethyl)styrene

https://huagongshe.com/reaction/15252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 23136688HCID 23136688—
SolventMethanolHCID 887—
SolventCarbon TetrachlorideHCID 5943—
Product3,5-Bis(chloromethyl)styreneHCID 2203382654%

Reaction Conditions

Temperature0 °C

Reaction Steps

Subsequently, 2.76 g (14.4 mmol) of 3,5-bis(methoxymethyl)styrene was dissolved in 30 ml of carbon tetrachloride in a reaction vessel of 200 ml, then 40 ml of methylene chloride solution containing 1.0 M boron trichloride was added dropwise at 0° C., and further agitated at 0° C. for 12 hours. After treating the excess boron trichloride by adding methanol to the reaction liquid, the resultant was poured into 150 ml of 5% NaOH solution (added with 100 g of ice). The organic layer was aliquoted and dried with anhydrous magnesium sulfate. Residues obtained by the removal of solvent were purified by silica gel column chromatography to obtain 1.57 g (7.81 mmol) of the target 3,5-bis(chloromethyl)styrene as a transparent liquid. Yield was 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732549B2
Source datasetuspto-grants-2010_06
ORD IDord-303c601ec63140ad9cb114983ef5fc0e
Source noteuspto-grants-2010_06