Identification | Back Directory | [Name]
2-BROMO-3-METHYLBENZONITRILE | [CAS]
263159-64-4 | [Synonyms]
2-BROMO-3-METHYLBENZONITRILE Benzonitrile, 2-bromo-3-methyl- 2-BroMo-3-Methylbenzonitrile 97% | [Molecular Formula]
C8H6BrN | [MDL Number]
MFCD09025664 | [MOL File]
263159-64-4.mol | [Molecular Weight]
196.04 |
Chemical Properties | Back Directory | [Melting point ]
67-71 °C | [Boiling point ]
286.8±28.0 °C(Predicted) | [density ]
1.51±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
powder | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
Step 2: To a solution of 2-bromo-3-methylbenzamide (12 g, 56.1 mmol) in N,N-dimethylformamide (DMF, 100 mL) was slowly added a solution of cyanuric chloride (15.47 g, 84.1 mmol) in DMF (50 mL) at 0 °C and under nitrogen protection. After addition, the reaction mixture was brought to room temperature and stirred overnight. Thin layer chromatography (TLC, unfolding agent: petroleum ether/ethyl acetate = 1:1) was monitored to show complete reaction. The reaction mixture was poured into water (500 mL) and extracted with ethyl acetate (EtOAc, 200 mL x 2). The organic phases were combined and washed sequentially with saturated aqueous sodium carbonate (200 mL × 2), saturated saline (200 mL × 4), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 2-bromo-3-methylbenzonitrile (11 g, 100% yield) as an off-white solid.1H NMR (400 MHz, CDCl3): δ 7.51-7.45 (m, 2H), 7.33 -7.29 (m, 1H), 2.47 (s, 3H). | [References]
[1] Patent: WO2013/132376, 2013, A1. Location in patent: Page/Page column 226 [2] Organic Letters, 2018, vol. 20, # 3, p. 728 - 731 [3] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 2, p. 644 - 651 [4] Patent: WO2011/22337, 2011, A1. Location in patent: Page/Page column 73-74 |
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Energy Chemical
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