HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971789Generated: October 26, 2026
Dichloromethane → 2-Bromo-5-(chloromethyl)-1,3-dimethoxybenzene
https://huagongshe.com/reaction/1971789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (4-Bromo-3,5-dimethoxyphenyl)methanol | HCID 11149289 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-5-(chloromethyl)-1,3-dimethoxybenzene | HCID 24971972 | — |
Reaction Steps
To a mixture of (4-bromo-3,5-dimethoxyphenyl)methanol (10.0 g, 40.6 mmol) and dichloromethane (100 mL) were added triethylamine (12.4 mL, 89.3 mmol) and methanesulfonyl chloride (3.46 mL, 44.7 mmol) in that order while cooling on ice, and the mixture was stirred at room temperature for 14 hours. Water was added to the mixture, and then ethyl acetate was added. After thoroughly shaking the mixture, the organic layer was separated and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (mixture of n-heptane and ethyl acetate: n-heptane/ethyl acetate=4/1) to obtain the title compound (2.47 g, 9.30 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431603B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-27fa93894c204e5092bc667ea1f8544b |
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| Source note | uspto-grants-2013_04 |
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