HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908892Generated: October 27, 2026
N-bromobutanimide → 4-Bromo-3-(bromomethyl)-5-methylphenyl acetate
https://huagongshe.com/reaction/1908892
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 | US08598226B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-5d39b46c408a4bb3b73cf782c7cbd8a2 |
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| Source note | uspto-grants-2013_12 |
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