HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516968Generated: October 26, 2026
Chlorobenzene → 1-(4-(Bromomethyl)-2-chlorophenyl)ethanone
https://huagongshe.com/reaction/516968
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(2-Chloro-4-methylphenyl)ethanone | HCID 15560949 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-(Bromomethyl)-2-chlorophenyl)ethanone | HCID 89853914 | 70% |
Reaction Steps
A mixture of 1-(2-chloro-4-methylphenyl)ethanone (1.6 g, 9.50 mmol) (preparation 15) and chlorobenzene (60 ml) was prepared at room temperature and N-bromosuccinimide (NBS) (1.86 g, 10.44 mmol) added followed by a catalytic amount of benzoyl peroxide (ca. 1.5 mg, 0.005 mmol), and the resulting mixture was heated to 140-145° C. for 16 h. The mixture was then allowed to cool to room temperature, diluted with toluene (50 ml) and filtered through a celite pad. The pad was washed with toluene (2×50 ml) and the filtrate concentrated under reduced pressure and purified by column chromatography (0-10% EtOAc/Hexanes) to afford 1-(4-(bromomethyl)-2-chlorophenyl)ethanone (1.65 g, 6.65 mmol, 70%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115088B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-63c8c2c23ef14ab3a813d19d099ced27 |
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| Source note | uspto-grants-2015_08 |
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