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N-bromobutanimide → 2-Methoxyphenyl 2-methoxy-3-bromomethylphenyl ether

HRID 1163976
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HRID 1163976 반응식
[Br:1]N1C(=O)CCC1=O.[CH3:9][O:10][C:11]1[C:16]([CH3:17])=[CH:15][CH:14]=[CH:13][C:12]=1[O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[O:25][CH3:26]>C1C=CC=CC=1.N(C(C)(C)C#N)=NC(C)(C)C#N>[CH3:9][O:10][C:11]1[C:16]([CH2:17][Br:1])=[CH:15][CH:14]=[CH:13][C:12]=1[O:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[O:25][CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 130666562-Methoxyphenyl 2-methoxy-3-methylphenyl ether

생성물 1

HCID 130666572-Methoxyphenyl 2-methoxy-3-bromomethylphenyl ether수율 101.6%

시약·촉매·용매 2

HCID 6547Azobisisobutyronitrile촉매HCID 241Benzene용매

실험 절차

N-Bromosuccinimide (6.56 g) and 2,2'-azobisisobutyronitrile (100 mg) were added to a solution of 2-methoxyphenyl 2-methoxy-3-methylphenyl ether (9.0 g) in benzene (100 ml), and the mixture was refluxed under heating for 2 hrs. The reaction mixture was evaporated, and water was added to the residue. The mixture was extracted with diethyl ether, and the extract was washed with water, dried over magnesium sulfate and then evaporated to give oily residue of 2-methoxyphenyl 2-methoxy-3-bromomethylphenyl ether (12.10 g).

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureunder heating for 2 hrs
  3. customThe reaction mixture was evaporated
  4. additionwater was added to the residue
  5. extractionThe mixture was extracted with diethyl ether
  6. washthe extract was washed with water
  7. dry with materialdried over magnesium sulfate
  8. customevaporated

출처 및 근거

ORD 기록
ord-04f85c56c26e4a01b2accc39660b98bd
출처 데이터셋
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04367238

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