HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15649Generated: October 31, 2026
N-bromobutanimide → 4-Bromo-3-(bromomethyl)-5-methylphenyl acetate
https://huagongshe.com/reaction/15649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Bromo-3,5-dimethylphenyl acetate | HCID 15184685 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-Bromo-3-(bromomethyl)-5-methylphenyl acetate | HCID 15184686 | 73% |
Reaction Steps
A suspension of 4-bromo-3,5-dimethylphenyl acetate (12.1 g, 49.8 mmol), N-bromosuccinimide (9.79 g, 55.0 mmol) and 2,2′-azobisisobutyronitrile (82.1 mg, 0.500 mmol) in carbon tetrachloride (100 mL) was stirred at 75° C. for 5 hr under nitrogen atmosphere. The reaction mixture was ice-cooled, and concentrated under reduced pressure. The residue was diluted with diethyl ether, the insoluble substance was filtered off, and the filtrate was concentrated under reduced pressure. The residue was-purified by silica gel column chromatography (ethyl acetate:hexane=0:100-25:75) to give the title compound (11.7 g, yield 73%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732626B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-6bd7035410354fee829adc3e25217709 |
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| Source note | uspto-grants-2010_06 |
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