ChemicalBook--->CAS DataBase List--->13599-24-1

13599-24-1

13599-24-1 Structure

13599-24-1 Structure
IdentificationBack 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 PropertiesBack 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
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 5-PHENYL-3-ISOXAZOLECARBOXYLATE(13599-24-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

ALPHA-CHLOROBENZALDOXIME

81745-44-0

Ethyl propiolate

623-47-2

ETHYL 5-PHENYL-3-ISOXAZOLECARBOXYLATE

13599-24-1

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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