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

HRID 21564
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인쇄 미리보기

반응식

HRID 21564 반응식
[Br:1]N1C(=O)CCC1=O.[O:9]1[CH:13]=[CH:12][C:11]([C:14]2[C:23]3[C:18](=[CH:19][C:20]([CH3:24])=[CH:21][CH:22]=3)[O:17][C:16](=[O:25])[CH:15]=2)=[CH:10]1.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:1][CH2:24][C:20]1[CH:19]=[C:18]2[C:23]([C:14]([C:11]3[CH:12]=[CH:13][O:9][CH:10]=3)=[CH:15][C:16](=[O:25])[O:17]2)=[CH:22][CH:21]=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 49.2%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

N-Bromosuccinimide (0.90 g, 5.06 mmol) was added to a stirred solution of the compound from Step 2 (1.04 g, 4.60 mmol) in CCl4 (150 ml) followed by a catalytic amount of azobis (isobutyronitrile). After the mixture was refluxed 3 h, the precipitated solid was removed by filtration and the solvent was evaporated in vacuo. The residue was stirred for 10 min in 15 ml Et2O, filtered and dried to give 0.69 g of the title compound. mp 155°-156° C.

후처리

  1. temperatureAfter the mixture was refluxed 3 h
  2. customthe precipitated solid was removed by filtration
  3. customthe solvent was evaporated in vacuo
  4. filtrationfiltered
  5. customdried

출처 및 근거

ORD 기록
ord-b463ae009edb49a39dd9696aea87e002
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05424320

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