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Chlorosuccinimide → HCID 15704073、化合物

HRID 1651517
ノート
印刷プレビュー

反応式

HRID 1651517 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 15704073HCID 15704073、化合物収率 84%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-31a62ec14130425ca414cebd4a2f40e4
出典データセット
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04929614

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート