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Azobisisobutyronitrile → 7-(Bromomethyl)-2-chloro-4-(4-fluorophenyl)quinoline

HRID 2422550
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인쇄 미리보기

반응식

HRID 2422550 반응식
[Cl:1][C:2]1[CH:11]=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=2)[C:9]2[C:4](=[CH:5][C:6]([CH3:19])=[CH:7][CH:8]=2)[N:3]=1.[Br:20]N1C(=O)CCC1=O.CC(N=NC(C#N)(C)C)(C#N)C>C(Cl)(Cl)(Cl)Cl>[Br:20][CH2:19][C:6]1[CH:5]=[C:4]2[C:9]([C:10]([C:12]3[CH:13]=[CH:14][C:15]([F:18])=[CH:16][CH:17]=3)=[CH:11][C:2]([Cl:1])=[N:3]2)=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 866219782-Chloro-4-(4-fluorophenyl)-7-methylquinoline

생성물 1

HCID 866219797-(Bromomethyl)-2-chloro-4-(4-fluorophenyl)quinoline

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

A solution of 2-chloro-4-(4-fluorophenyl)-7-methylquinoline (2.0 g, 7.4 mmol), N-bromo-succinimide (1.57 g, 8.8 mmol) and AIBN (30 mg, 0.18 mmol) in CCl4 (40 mL) was refluxed for 16 h. The solution was then cooled to rt, filtered and concentrated. Purification on silica gel (eluting with dichloromethane/hexanes, 1:1) gave the title compound. MS (+ESI): 351 (M+H)+.

후처리

  1. filtrationfiltered
  2. concentrationconcentrated
  3. customPurification on silica gel (eluting with dichloromethane/hexanes, 1:1)

출처 및 근거

ORD 기록
ord-9238ea38c98849b290a508295201496e
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960409B2

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