Identification | Back Directory | [Name]
5-CHLORO-2-(TRIFLUOROMETHYL)BENZALDEHYDE | [CAS]
90381-07-0 | [Synonyms]
Benzaldehyde, 5-chloro-2-(trifluoromethyl)- | [Molecular Formula]
C8H4ClF3O | [MDL Number]
MFCD03412204 | [MOL File]
90381-07-0.mol | [Molecular Weight]
208.57 |
Chemical Properties | Back Directory | [Boiling point ]
82-86℃ | [density ]
1.423±0.06 g/cm3(Predicted) | [refractive index ]
1.4880 | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
liquid | [color ]
Clear, colourless | [Sensitive ]
Air Sensitive |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 5-chloro-2-trifluoromethylbenzaldehyde from (5-chloro-2-trifluoromethylphenyl)methanol: (5-chloro-2-trifluoromethylphenyl)methanol (347 mg, 1.66 mmol) was dissolved in dichloromethane (10 mL). Pyridinium chlorochromate (717 mg, 3.32 mmol) was added to the solution and the reaction mixture was stirred for 2 hours at room temperature. After the reaction was completed, the reaction solution was diluted with ether and stirring was continued for 1 hour. Subsequently, the reaction mixture was filtered to remove insoluble impurities and the filtrate was concentrated to remove solvent. Finally, the crude product was purified by silica gel column chromatography using a hexane solution of 10% ethyl acetate as eluent to afford 5-chloro-2-trifluoromethylbenzaldehyde as a colorless oil (285 mg, 82% yield).1H NMR (400 MHz, MeOH-d4) δ 10.33 (s, 1H), 7.90 (s, 1H), 7.69 (d, 1H, J = 8.4 Hz), 7.54 (d, 1H, J = 8.4 Hz). | [References]
[1] Patent: WO2006/44454, 2006, A1. Location in patent: Page/Page column 13-14 |
|
|