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Azobisisobutyronitrile → 7-Bromomethyl-4-(3-furyl)coumarin

HRID 741827
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반응식

HRID 741827 반응식
[O:1]1[CH:5]=[CH:4][C:3]([C:6]2[C:15]3[C:10](=[CH:11][C:12]([CH3:16])=[CH:13][CH:14]=3)[O:9][C:8](=[O:17])[CH:7]=2)=[CH:2]1.C1C(=O)N([Br:25])C(=O)C1.CC(N=NC(C#N)(C)C)(C#N)C>C(Cl)(Cl)(Cl)Cl>[Br:25][CH2:16][C:12]1[CH:11]=[C:10]2[C:15]([C:6]([C:3]3[CH:4]=[CH:5][O:1][CH:2]=3)=[CH:7][C:8](=[O:17])[O:9]2)=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 67184N-bromobutanimideHCID 233701904-(3-Furyl)-7-methylcoumarin

생성물 1

HCID 157805647-Bromomethyl-4-(3-furyl)coumarin수율 42.2%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

To a solution of 4-(furan-3-yl)-7-methylcoumarin (1.2 g, 5.3 mmol) in CCl4 (40 mL) was added NBS(1 g, 5.8 mmol) followed by AIBN (87 mg, 0.53 mmol). The resulting mixture was refluxed for 4 h, then cooled to r.t. filtered and evaporated. Purification by chromatrography on silica gel gave 682 mg (42%) of the title compound.

후처리

  1. temperatureThe resulting mixture was refluxed for 4 h
  2. filtrationfiltered
  3. customevaporated
  4. customPurification by chromatrography on silica gel

출처 및 근거

ORD 기록
ord-0a17468180b4435fb954f5db2dd921d5
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05552437

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