HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15252Generated: October 31, 2026
Dichloromethane → 3,5-Bis(chloromethyl)styrene
https://huagongshe.com/reaction/15252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 23136688 | HCID 23136688 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3,5-Bis(chloromethyl)styrene | HCID 22033826 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732549B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-303c601ec63140ad9cb114983ef5fc0e |
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| Source note | uspto-grants-2010_06 |
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