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Water → (4-Bromo-7-methoxybenzofuran-2-yl)-cyclopropyl-methanone

HRID 1108303
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HRID 1108303 반응식
[Br:1]N1C(=O)CCC1=O.[CH:9]1([C:12]([C:14]2[O:15][C:16]3[C:22]([O:23][CH3:24])=[CH:21][CH:20]=[CH:19][C:17]=3[CH:18]=2)=[O:13])[CH2:11][CH2:10]1.O>C(#N)C>[Br:1][C:19]1[C:17]2[CH:18]=[C:14]([C:12]([CH:9]3[CH2:10][CH2:11]3)=[O:13])[O:15][C:16]=2[C:22]([O:23][CH3:24])=[CH:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 67184N-bromobutanimideHCID 18784859Cyclopropyl-(7-methoxybenzofuran-2-yl)-methanone

생성물 1

HCID 18784855(4-Bromo-7-methoxybenzofuran-2-yl)-cyclopropyl-methanone수율 70.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

N-bromosuccinimide (0.21 g) was added in a single portion to a stirred solution of cyclopropyl-(7-methoxybenzofuran-2-yl)-methanone (0.25 g) in acetonitrile (20 ml) under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 24 h. Water (20 ml) was added, the mixture extracted with ethyl acetate (100 ml), the organic layer separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with 5-10% ethyl acetate in hexane afforded the title compound as an off-white solid (0.24 g).

후처리

  1. extractionthe mixture extracted with ethyl acetate (100 ml)
  2. customthe organic layer separated
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customPurification by flash chromatography on silica eluting with 5-10% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-5bf4a7643b024c5b913e075851dc6d83
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06066657

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