Triethylamine → 5-Chloro-3-phenylisoxazole

HRID 1195792노트

반응식

HRID 1195792 반응식
P(Cl)(Cl)([Cl:3])=O.[C:6]1([C:12]2[NH:13][O:14][C:15](=O)[CH:16]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.C(N(CC)CC)C>>[C:6]1([C:12]2[CH:16]=[C:15]([Cl:3])[O:14][N:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

참가 물질

4

실험 절차

To 84.3 g (0.55 mol) of phosphorus oxychloride, 18.3 g (0.11 mol) of 3-phenyl-5-isoxazolone were added under stirring. While the internal temperature was maintained at 0°-10.C., 11.1 g (0.11 mol) of triethylamine were added further. They were then reacted under heating and stirring at 100°-120° C. for 3 hours. The reaction mixture was allowed to stand overnight at room temperature, and precipitated insoluble matter was filtered off. After the filtrate thus obtained was concentrated under reduced pressure, the residue was transferred into 500 ml of ice water, followed by neutralization with sodium hydrogencarbonate. The solution was extracted with ethyl ether. The organic layer was washed with water and then dried. The solvent was distilled off and the residue was purified by silica gel column chromatography (solvent: hexane/ethyl acetate=20/1), whereby the title compound was obtained as colorless crystals.

후처리

  1. customThey were then reacted
  2. temperatureunder heating
  3. stirringstirring at 100°-120° C. for 3 hours
  4. customprecipitated insoluble matter
  5. filtrationwas filtered off
  6. customAfter the filtrate thus obtained
  7. concentrationwas concentrated under reduced pressure
  8. extractionThe solution was extracted with ethyl ether
  9. washThe organic layer was washed with water
  10. customdried
  11. distillationThe solvent was distilled off
  12. customthe residue was purified by silica gel column chromatography (solvent: hexane/ethyl acetate=20/1), whereby the title compound
  13. customwas obtained as colorless crystals

출처 및 근거

ORD 기록
ord-2b8cb48b9f0d458ba2062ba1ff0ac972
출처 데이터셋
uspto-grants-1992_05
특허 번호
US05112841

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