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| 2-ACETYLBENZALDEHYDE 95 Basic information |
Product Name: | 2-ACETYLBENZALDEHYDE 95 | Synonyms: | 2-ACETYLBENZALDEHYDE 95;Benzaldehyde, o-acetyl-;Ortho-acetylbenzaldehyde;2-Acetylbenzaldehyde,2-Formylacetophenone;2-Acetylbenzaldehyde 95%;Benzaldehyde, 2-acetyl- | CAS: | 24257-93-0 | MF: | C9H8O2 | MW: | 148.16 | EINECS: | | Product Categories: | | Mol File: | 24257-93-0.mol |  |
| 2-ACETYLBENZALDEHYDE 95 Chemical Properties |
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 |
WGK Germany | 3 | HS Code | 2914409000 |
| 2-ACETYLBENZALDEHYDE 95 Usage And Synthesis |
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 |
| 2-ACETYLBENZALDEHYDE 95 Preparation Products And Raw materials |
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