HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440538Generated: October 25, 2026
4-Chloro-3-methylphenol → 2-(Bromomethyl)-1-chloro-4-methoxybenzene
https://huagongshe.com/reaction/440538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3-methylphenol | HCID 1732 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(Bromomethyl)-1-chloro-4-methoxybenzene | HCID 12484533 | — |
Reaction Steps
Methyl iodide (110 g was added dropwise to a stirred solution of 4-chloro-3-methylphenol (100 g) and potassium carbonate (194 g) in acetone (500 ml). The mixture was stirred for 1.5 hours. Methyl iodide (142 g) was added and the mixture stirred for a further hour. Solvent was removed by evaporation and the residue partitioned between water and ethyl acetate. The organic layer yielded an oil which was heated under reflux for 2 hours with N-bromosuccinimide (119 g) and benzoyl peroxide (1 g) in carbon tetrachloride (250 ml). The mixture was cooled, filtered and the filtrate concentrated to give a residue which was distilled under high vacuum. The fractions collected between 88° and 94° C./0.4 mbar were recrystallised from petroleum ether (b.p. 60°-80° C.) to give 2-chloro-5-methoxy benzyl bromide, m.p. 51°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05519034 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-1d535b203d78433f9de20e65f2021495 |
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| Source note | uspto-grants-1996_05 |
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