Identification | Back Directory | [Name]
2-ACETYLBENZALDEHYDE 95 | [CAS]
24257-93-0 | [Synonyms]
Benzaldehyde, o-acetyl- Benzaldehyde, 2-acetyl- Ortho-acetylbenzaldehyde 2-ACETYLBENZALDEHYDE 95 2-Acetylbenzaldehyde 95% 2-Acetylbenzaldehyde,2-Formylacetophenone | [Molecular Formula]
C9H8O2 | [MDL Number]
MFCD05865162 | [MOL File]
24257-93-0.mol | [Molecular Weight]
148.16 |
Chemical Properties | Back Directory | [Melting point ]
39-43 °C (lit.) | [Boiling point ]
268.8±23.0 °C(Predicted) | [density ]
1.117±0.06 g/cm3(Predicted) | [Fp ]
>230 °F | [storage temp. ]
2-8°C, stored under nitrogen | [form ]
crystalline solid | [color ]
White/off-white |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 2-acetylbenzaldehyde using 2-ethynylbenzaldehyde as starting material: the general method was as follows: first, AgBArF (97.1 mg, 0.1 mmol) was accurately weighed and placed in a long-necked glass reactor, followed by the addition of 2-ethynylbenzaldehyde (1 mmol). Next, 10 μL of ethyl acetate (EtOAc) was added and stirred for 5 min. After that, n-dodecane (1 mmol), an internal standard, and 3 mL of deionized water were added, and the reaction device was placed in an oil bath at 80 °C with continuous stirring and heated for 12 to 24 hours. Upon completion of the reaction, the reaction device was opened and 3 mL of ethyl acetate (EtOAc) was added to it and stirred for 5 minutes, after which the organic phase was separated and collected. The organic phase was passed through a short silica gel column to remove possible impurities and subsequently analyzed by GC-MS. Finally, the product was purified by silica gel column chromatography using a hexane/ethyl acetate (EtOAc) solvent mixture as eluent. The purified product was structurally characterized by 1H NMR and ESI-MS. | [References]
[1] Tetrahedron Letters, 2014, vol. 55, # 8, p. 1444 - 1447 |
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