Azobisisobutyronitrile → 2-(Bromomethyl)-3-chlorobenzonitrile

HRID 1681941

반응식

HRID 1681941 반응식
[Cl:1][C:2]1[C:3]([CH3:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[C:5]#[N:6].[Br:11]N1C(=O)CCC1=O.CC(N=NC(C#N)(C)C)(C#N)C>C(Cl)(Cl)(Cl)Cl.C(Cl)Cl>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:4]([C:5]#[N:6])[C:3]=1[CH2:10][Br:11]

참가 물질

6

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 5215083-Chloro-2-methylbenzonitrile

생성물 1

HCID 149805102-(Bromomethyl)-3-chlorobenzonitrile수율 46%

시약·촉매·용매 2

HCID 5943Carbon Tetrachloride용매HCID 6344Dichloromethane용매

실험 절차

To a refluxing solution of 3-chloro-2-methylbenzonitrile (2.0 g,13.2 mmol) in 20 mL of CCl4 was added 2.6 g (14.4 mmol, 1.1 eq) of N-bromosuccinimide and 0.2 g of AIBN. The solution was refluxed for 3 hours and then cooled, diluted with 500 mL of CH2Cl2 and washed with 200 mL of H2O and 200 mL of brine. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The resultant oil was flash chromatographed with 5:1 hexane/ethyl acetate to yield the titled compound (1.4 g, 46%) as a yellow oil.

후처리

  1. temperatureThe solution was refluxed for 3 hours
  2. temperaturecooled
  3. washwashed with 200 mL of H2O and 200 mL of brine
  4. dry with materialThe organic phase was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customchromatographed with 5:1 hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-3b546b47d34b473092825a58018d0021
출처 데이터셋
uspto-grants-1992_12
특허 번호
US05175164

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