HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643352Generated: October 31, 2026
N-bromobutanimide → 1-Bromo-3-(bromomethyl)-5-methylbenzene
https://huagongshe.com/reaction/1643352
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzene, 1-bromo-3,5-dimethyl- | HCID 136357 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-Bromo-3-(bromomethyl)-5-methylbenzene | HCID 22324261 | 94.2% |
Reaction Steps
A mixture of 3,5-dimethylbromobenzene (70 g, 0.378 M), NBS (67.3 g, 0.373 M), and benzoyl peroxide (2.27 g, 0.009 M) in carbon tetrachloride (300 mL) was refluxed for 3 hr. After cooling to room temperature, the mixture was filtered and the filtrate was evaporated in vacuo to give a pale brown oil. The crude product was dissolved in hexane and filtered through a short silica gel pad (diameter: 9.5 cm, height: 7 cm). The silica gel pad was washed with hexane until the product eluted completely. The filtrate was evaporated in vacuo to give 94 g of 1-bromo-3-(bromomethyl)-5-methylbenzene (contaminated with starting material and 1-bromo-3,5-bis-bromomethylbenzene) as a pale brown oil, which solidified on standing at room temperature. The mixture was used directly in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119800B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-d89c5f57c1684aa5b7c64b5fc0d5f365 |
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| Source note | uspto-grants-2012_02 |
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