HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425939Generated: October 29, 2026
Benzoyl Peroxide → 1-Bromo-2-(bromomethyl)-3-(trifluoromethyl)benzene
https://huagongshe.com/reaction/1425939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Bromo-2-methyl-3-(trifluoromethyl)benzene | HCID 2775634 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-Bromo-2-(bromomethyl)-3-(trifluoromethyl)benzene | HCID 22754136 | 99% |
Reaction Steps
To a solution of 1-bromo-2-methyl-3-(trifluoromethyl)benzene (CXXVII) (5.7 g, 23.86 mmol) in CCl4 (50 mL) was added NBS (4.24 g, 23.86 mmol) and a catalytic amount of benzoyl peroxide. The reaction mixture was gently refluxed for 1 h. The reaction mixture was cooled to room temperature and the precipitate was removed by filtration. The solution was concentrated under reduced pressure and the crude product was dissolved in hexane and additional precipitate was removed by filtration. The filtrate was concentrated to dryness to give 1-bromo-2-(bromomethyl)-3-(trifluoromethyl)benzene (CXXVIII) as an orange oil (7.51 g, 23.62 mmol). 1H NMR (DMSO-d6) δ ppm 4.73 (s, 2H), 7.4 (dd, J=8 Hz, J=8 Hz, 1H), 7.80 (d, J=8 Hz, 1H), 8.02 (d, J=8 Hz, 1H); 19F NMR (DMSO-d6) δ ppm −57.85 (s, 3F). The crude product was used without further purification for step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933018B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-0cdb4fbb43a047a7b58ce292db816977 |
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| Source note | uspto-grants-2015_01 |
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