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Ethyl Acetate → HCID 14370871, 화합물

HRID 1199602
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인쇄 미리보기

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HRID 1199602 반응식
[F:1][C:2]1[CH:8]=[C:7]([Br:9])[C:6]([O:10][C:11]([O:13][CH3:14])=[O:12])=[CH:5][C:3]=1[NH2:4].[C:15](OCC)(=[O:17])C>>[F:1][C:2]1[CH:8]=[C:7]([Br:9])[C:6]([O:10][C:11]([O:13][CH3:14])=[O:12])=[CH:5][C:3]=1[N:4]=[C:15]=[O:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 8857Ethyl Acetate2회HCID 14370869HCID 14370869, 화합물

생성물 1

HCID 14370871HCID 14370871, 화합물수율 94%

반응 조건

온도
80 °C

실험 절차

A solution of trichloromethyl chloroformate trichloromethyl (15 ml, 125 mmol) in ethyl acetate was charged into a 500 ml-three neck flask equipped with a dropping funnel and distillation apparatus and, a solution of 2-fluoro-4-bromo-5-methoxycarbonyloxyaniline (28.0 g,113 mmol) in ethyl acetate (100 ml) was added dropwise over 20 minutes. After dropping, the mixture was heated at 80° C. and ethyl acetate was removed by distillation. After cooling, carbon tetrachloride (150 ml) was added and the undissolved substances were removed by filtration. The solvent was then removed from the filtrate by distillation under reduced pressure, whereby a brown solid of 2-fluoro-4-bromo-5-methoxycarbonyloxyphenyl isocyanate (29.1 g, yield 94%) was obtained.

후처리

  1. customequipped with a dropping funnel
  2. distillationdistillation apparatus
  3. customethyl acetate was removed by distillation
  4. temperatureAfter cooling
  5. additioncarbon tetrachloride (150 ml) was added
  6. customthe undissolved substances were removed by filtration

출처 및 근거

ORD 기록
ord-6b8ccc9400fa4e49b92fb48100c5052e
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04902337

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