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Chlorosuccinimide → 5-Chloro-1-(4-cyanophenyl)-2-methylimidazole

HRID 1085148
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인쇄 미리보기

반응식

HRID 1085148 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH:13]=[CH:12][N:11]=[C:10]2[CH3:14])=[CH:5][CH:4]=1)#[N:2].[Cl:15]N1C(=O)CCC1=O>C(Cl)(Cl)Cl>[Cl:15][C:13]1[N:9]([C:6]2[CH:5]=[CH:4][C:3]([C:1]#[N:2])=[CH:8][CH:7]=2)[C:10]([CH3:14])=[N:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 150053844-(2-Methyl-1H-imidazol-1-yl)benzonitrile

생성물 1

HCID 200610385-Chloro-1-(4-cyanophenyl)-2-methylimidazole

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of 1-(4-cyanophenyl)-2-methylimidazole (3 g, 16.4 mmol) and N-chlorosuccinimide (2.18 g, 16.3 mmol) in chloroform (180 ml) was heated at reflux for 4 hours, then washed with water, dried over magnesium sulphate and evaporated to a yellow solid. Trituration with ether left a pale-yellow solid (2.38 g, 67%).

후처리

  1. temperatureat reflux for 4 hours
  2. washwashed with water
  3. dry with materialdried over magnesium sulphate
  4. customevaporated to a yellow solid
  5. waitTrituration with ether left a pale-yellow solid (2.38 g, 67%)

출처 및 근거

ORD 기록
ord-8129d1d277e145ec8eda82bcf372b7db
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05008263

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