Identification | Back Directory | [Name]
2-(2-Bromophenyl)-2-methylpropanenitrile | [CAS]
57775-06-1 | [Synonyms]
2-(2-Bromophenyl)-2-methylpropanenitrile 2-(2-Bromo-phenyl)-2-methyl-propionitrile Benzeneacetonitrile, 2-bromo-α,α-dimethyl- | [Molecular Formula]
C10H10BrN | [MDL Number]
MFCD11036582 | [MOL File]
57775-06-1.mol | [Molecular Weight]
224.1 |
Chemical Properties | Back Directory | [Boiling point ]
95-105 °C(Press: 0.03 Torr) | [density ]
1.352±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [Appearance]
Colorless to light yellow Liquid |
Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 2-(2-bromophenyl)-2-methylpropionitrile from o-bromofluorobenzene and isobutyronitrile was as follows: in a Mettler Toledo MiniBlock reaction tube, 0.01 mol of 1-bromo-2-fluorobenzene and a solution of 2-methylpropionitrile prepared from 14 g of formononitrile in 8.5 mL of THF with 160 mL of THF were added separately. Subsequently, an equimolar amount (0.01 mol) of sodium hexamethyldisilanilide (1 M solution in THF) was added as a base to each reaction tube at ambient temperature. The reaction mixture was heated to 65 °C over 1 h, then cooled to ambient temperature and the reaction was quenched with 6 mL of 5% HCl solution. The organic phase was separated and the solvent was removed by evaporation. The crude product was analyzed by gas chromatography (GC)/mass spectrometry (MS) and proton nuclear magnetic resonance (1H-NMR) to give 2-(2-bromophenyl)-2-methylpropanenitrile (5.2% GC/MS yield) and unreacted haloaromatics (76.8%). | [References]
[1] Patent: US2006/247441, 2006, A1. Location in patent: Page/Page column 17 |
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Energy Chemical
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http://www.energy-chemical.com |
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