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335013-18-8

335013-18-8 Structure

335013-18-8 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2902900000
Spectrum DetailBack Directory
[Spectrum Detail]

4-broMo-1-(broMoMethyl)-2-(trifluoroMethyl)benzene(335013-18-8)1HNMR
4-broMo-1-(broMoMethyl)-2-(trifluoroMethyl)benzene(335013-18-8)FT-IR
Hazard InformationBack Directory
[Synthesis]

4-METHYL-3-(TRIFLUOROMETHYL)BROMOBENZENE

86845-27-4

4-broMo-1-(broMoMethyl)-2-(trifluoroMethyl)benzene

335013-18-8

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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