Identification | Back Directory | [Name]
ETHYL 5-PHENYL-3-ISOXAZOLECARBOXYLATE | [CAS]
13599-24-1 | [Synonyms]
TIMTEC-BB SBB014614 ethyl 3-phenyl-5-isoxazolecarboxylate | [Molecular Formula]
C12H11NO3 | [MDL Number]
MFCD01596796 | [MOL File]
13599-24-1.mol | [Molecular Weight]
217.22 |
Chemical Properties | Back Directory | [Melting point ]
47 °C | [Boiling point ]
379.8±30.0 °C(Predicted) | [density ]
1.173±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
-4.43±0.50(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of ethyl 3-phenylisoxazole-5-carboxylate from (E)-N-hydroxybenzimidoyl chloride and ethyl propargylate: preparation of the intermediate 54-ethyl S-phenylisoxazole-δ-carboxylic acid ethyl ester. The reaction was carried out by stirring ethyl propiolate (0.657 mL, 6.43 mmol), (E)-N-hydroxybenzenecarboximidoyl chloride (0.500 g, 3.21 mmol), and sodium bicarbonate (0.818 g, 9.64 mmol) in a mixed solvent of ethyl acetate (16 mL) and water (1 mL) at room temperature overnight. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The crude product was purified by fast column chromatography on silica gel, the eluent being a heptane solution of 5% to 80% dichloromethane, to give 0.295 g of ethyl 3-phenylisoxazole-5-carboxylate in 42% yield.ESI/APCI (+): 218 (M + H). | [References]
[1] Patent: WO2010/142801, 2010, A1. Location in patent: Page/Page column 162-163 |
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Company Name: |
SynAsst Chemical.
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021-60343070 |
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www.chemicalbook.com/ShowSupplierProductsList15848/0_EN.htm |
Company Name: |
Biokitchen
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021-021-021-31663258 13795219287 |
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www.chemicalbook.com/ShowSupplierProductsList20174/0_EN.htm |
Company Name: |
Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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