Identification | More | [Name]
4-FLUOROPHENYLGLYOXAL HYDRATE | [CAS]
447-43-8 | [Synonyms]
4-FLUOROPHENYLGLYOXAL HYDRATE 4-FLUOROPHENYLGLYOXAL MONOHYDRATE 2-(4-Fluorophenyl)-2-oxo-acetaldehyde 2-(4-fluorophenyl)-2-oxoacetaldehyde hydrate 4-FLUOROPHENYLGLYOXAL HYDRATE , DRY WT. BASIS 4-FLUOROPHENYLGLYOXAL HYDRATE, 98%, DRY WT. BASIS | [EINECS(EC#)]
639-289-9 | [Molecular Formula]
C8H7FO3 | [MDL Number]
MFCD01320770 | [Molecular Weight]
170.14 | [MOL File]
447-43-8.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [RTECS ]
CY1440000 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
2914790090 |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of hydrated 4-fluorobenzoylformaldehyde from 4-fluoroacetophenone: general method: a mixture of substrate (0.6 mmol) and bromoethylene (2a, 0.06 mmol) in DMSO (1.1 mL) was placed in an open-topped flask and heated in an oil bath (see Table 2 for specific temperatures and reaction times). After completion of the reaction (monitored by TLC), the reaction mixture was diluted with water (11 mL), treated with saturated NaCl solution and extracted with ethyl acetate (5 × 4 mL). Only in case of synthesis of arylglyoxal, the organic layer was additionally washed with Na2CO3 solution (0.12 mmol, dissolved in 2 mL of water), followed by saturated aqueous NaCl solution and dried with anhydrous Na2SO4. The extract was purified by column chromatography (eluent: petroleum ether/ethyl acetate gradient) to give pure product. | [References]
[1] Chinese Chemical Letters, 2013, vol. 24, # 12, p. 1118 - 1122 [2] Tetrahedron, 2011, vol. 67, # 41, p. 8000 - 8008 [3] Chemistry of Heterocyclic Compounds, 2018, vol. 54, # 1, p. 51 - 57 [4] Khim. Geterotsikl. Soedin., 2018, vol. 54, # 1, p. 51 - 57,7 [5] Journal of Organic Chemistry, 1952, vol. 17, p. 1425,1429 |
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