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Chlorosuccinimide → HCID 15704073, 화합물

HRID 1651517
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HRID 1651517 반응식
[F:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[C:4]([C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:14]=1[NH:13][CH2:12][CH2:11]2)=[O:5].[Cl:19]N1C(=O)CCC1=O>C(Cl)Cl>[Cl:19][C:8]1[CH:9]=[C:10]2[C:14](=[C:6]([C:4](=[O:5])[C:3]3[CH:15]=[CH:16][CH:17]=[CH:18][C:2]=3[F:1])[CH:7]=1)[NH:13][CH2:12][CH2:11]2
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 15704064(2,3-Dihydro-1H-indol-7-yl)(2-fluorophenyl)methanone

생성물 1

HCID 15704073HCID 15704073, 화합물수율 84%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

44 g (182 mmol) of 7-(2-fluorobenzoyl)indoline and 800 ml of methylene chloride are poured into a reactor equipped with a central stirrer, a condenser provided with a calcium chloride guard tube, a dipping thermometer, a nitrogen inlet and a pressure-equalizing dropping funnel. 27.9 g (182 mmol) of N-chlorosuccinimide are added gradually and the mixture is stirred over a warm temperature. The mixture is washed with saturated sodium bicarbonate solution and then with water, dried and evaporated. It is chromatographed on silica, eluting with methylene chloride. 42 g (84% yield) are obtained. The product is obtained in the form of a foam which has no definite melting point. TLC: H2CCl2Rf=0.70.

후처리

  1. customequipped with a central stirrer, a condenser
  2. customprovided with a calcium chloride guard tube
  3. washThe mixture is washed with saturated sodium bicarbonate solution
  4. dry with materialwith water, dried
  5. customevaporated
  6. customIt is chromatographed on silica
  7. washeluting with methylene chloride
  8. custom42 g (84% yield) are obtained
  9. customThe product is obtained in the form of a foam which

출처 및 근거

ORD 기록
ord-31a62ec14130425ca414cebd4a2f40e4
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04929614

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