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864274-04-4

864274-04-4 Structure

864274-04-4 Structure
IdentificationBack Directory
[Name]

2-Methylbenzo[d]oxazole-6-carbaldehyde
[CAS]

864274-04-4
[Synonyms]

2-methyl-6-benzoxazolecarboxaldehyde
6-Benzoxazolecarboxaldehyde, 2-methyl-
2-Methylbenzo[d]oxazole-6-carbaldehyde
[Molecular Formula]

C9H7NO2
[MDL Number]

MFCD20528168
[MOL File]

864274-04-4.mol
[Molecular Weight]

161.16
Chemical PropertiesBack Directory
[Boiling point ]

282.2±13.0 °C(Predicted)
[density ]

1.263±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

0.08±0.30(Predicted)
[Appearance]

White to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methylbenzo[d]oxazole-6-carbaldehyde(864274-04-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

(2-Methylbenzo[d]oxazol-6-yl)Methanol

136663-40-6

2-Methylbenzo[d]oxazole-6-carbaldehyde

864274-04-4

c) Synthesis of 2-methylbenzo[d]oxazole-6-carbaldehyde; To a solution of (2-methylbenzo[d]oxazol-6-yl)methanol (12.5 g, 76 mmol) in dichloromethane (200 mL) was added pyridinium chlorochromate (20 g, 93 mmol, 1.2 equiv.) and the reaction mixture was stirred for 1 h at room temperature. Diatomaceous earth (10 g) and activated carbon (2 g) were added to decolorize the mixture, which was filtered after continued stirring for 15 min. After evaporation of the solvent, the crude product was purified by column chromatography (eluent ratio 1:10 ethyl acetate:dichloromethane) to give 8.2 g (66% yield) of pure 2-methylbenzo[d]oxazole-6-carboxaldehyde.1H-NMR (CDCl3): δ 2.73 (s, 3H), 7.79 (d, 1H, J = 8.1 Hz), 7.88 (dd, 1H, J = 8.1 Hz, J' = 1.2 Hz), 8.03 (d, 1H, J = 1.2 Hz), 10.09 (s, 1H).LC-MS (m/z): 162.2 (MH+). Retention time (Rt): 1.47 min.

[References]

[1] Patent: WO2005/82901, 2005, A1. Location in patent: Page/Page column 33; 61-62
[2] Patent: WO2007/103755, 2007, A2. Location in patent: Page/Page column 81; 83
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