Identification | Back Directory | [Name]
4-Bromo-2-cyanobenzaldehyde | [CAS]
523977-64-2 | [Synonyms]
4-Bromo-2-cyanobenzaldehyde 5-Bromo-2-formylbenzonitrile 2-Cyano-4-bromo-benzaldehyde Benzonitrile, 5-bromo-2-formyl- | [Molecular Formula]
C8H4BrNO | [MDL Number]
MFCD09261030 | [MOL File]
523977-64-2.mol | [Molecular Weight]
210.03 |
Chemical Properties | Back Directory | [Boiling point ]
324℃ | [density ]
1.65 | [Fp ]
150℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
solid | [Appearance]
Off-white to light brown Solid |
Hazard Information | Back Directory | [Application]
4-Bromo-2-cyanobenzaldehyde is a useful research chemical. | [Synthesis]
General procedure for the synthesis of 4-bromo-2-cyanobenzaldehyde from 5-bromo-2-(bromomethyl)benzonitrile: To a stirred solution of trimethylamine N-oxide dihydrate (16.98 g, 152.8 mmol) in DMSO (60 mL) was added 5-bromo-2-(bromomethyl)benzonitrile (from step 1, 10.5 g, 38.19 mmol) in DCM (30 mL) to the solution in DCM. The resulting mixture was added slowly at 5 °C, followed by warming to 22 °C and continued stirring for 6 hours. After completion of the reaction, the reaction mixture was diluted with DCM (70 mL), washed sequentially with brine (20 mL × 3), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel column chromatography (eluent: 0-16% EtOAc in petroleum ether solution) to afford 4-bromo-2-cyanobenzaldehyde (4.2 g, 52% yield) as a white solid.1H NMR (400 MHz, CDCl3) δ 10.31 (s, 1H), 7.98 (s, 1H), 7.92 (s, 2H). | [References]
[1] Organic Letters, 2003, vol. 5, # 7, p. 1131 - 1134 [2] Journal of Materials Chemistry, 2011, vol. 21, # 26, p. 9523 - 9531 [3] Patent: US2017/362228, 2017, A1. Location in patent: Paragraph 0466; 0467 |
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