Benzoyl Peroxide → 1-Bromo-2-(bromomethyl)-3-(trifluoromethyl)benzene

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.

1. temperatureThe reaction mixture was gently refluxed for 1 h
2. customthe precipitate was removed by filtration
3. concentrationThe solution was concentrated under reduced pressure
4. dissolutionthe crude product was dissolved in hexane
5. customadditional precipitate was removed by filtration
6. concentrationThe filtrate was concentrated to dryness

ORDレコード

ord-0cdb4fbb43a047a7b58ce292db816977

出典データセット

uspto-grants-2015_01

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08933018B2