Identification | Back Directory | [Name]
4-broMo-1-(broMoMethyl)-2-(trifluoroMethyl)benzene | [CAS]
335013-18-8 | [Synonyms]
4-Bromo-2-(trifluoromethyl)benzyl bromide 95% 4-broMo-1-(broMoMethyl)-2-(trifluoroMethyl)benzene Benzene, 4-bromo-1-(bromomethyl)-2-(trifluoromethyl)- | [Molecular Formula]
C8H5Br2F3 | [MDL Number]
MFCD13185414 | [MOL File]
335013-18-8.mol | [Molecular Weight]
317.93 |
Chemical Properties | Back Directory | [Boiling point ]
239.4±35.0 °C(Predicted) | [density ]
1.885±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
liquid | [color ]
Colorless |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 4-bromo-1-(bromomethyl)-2-(trifluoromethyl)benzene from 5-bromo-2-methyltrifluorotoluene: 5-bromo-2-methyltrifluorotoluene (25 g, 104.59 mmol), N-bromosuccinimide (18.62 g, 104.59 mmol) and benzoyl peroxide (1.27 g, 5.23 mmol) were reacted in a A mixture in carbon tetrachloride (35 mL) was heated and reacted at 90 °C for 4 hours. Upon completion of the reaction, the mixture was cooled to 0 °C and filtered through a glass sand core funnel and the solids were washed with dichloromethane. The filtrates were combined and concentrated and subsequently purified by fast column chromatography (eluent: hexane/ethyl acetate, 0% to 5% ethyl acetate gradient) to give a clear oily product, which was crystallized after standing (33.26 g, 100% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 4.57 (s, 2H), 7.46 (d, J = 8.3 Hz, 1H), 7.67 (d, J = 8.3 Hz, 1H), 7.78 (s, 1H). | [References]
[1] Patent: WO2006/18725, 2006, A1. Location in patent: Page/Page column 208 [2] Journal of Labelled Compounds and Radiopharmaceuticals, 2015, vol. 58, # 5, p. 188 - 195 [3] Patent: WO2008/148867, 2008, A2. Location in patent: Page/Page column 37 [4] Patent: WO2009/23964, 2009, A1. Location in patent: Page/Page column 24 [5] Patent: WO2006/46593, 2006, A1. Location in patent: Page/Page column 235 |
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