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Dichloromethane → 4,5-dibromo-2-(4-hydroxyphenyl)-2H-pyridazin-3-one

HRID 15047
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인쇄 미리보기

반응식

HRID 15047 반응식
ClCCl.B(Br)(Br)Br.[Br:8][C:9]1[C:10](=[O:24])[N:11]([C:16]2[CH:21]=[CH:20][C:19]([O:22]C)=[CH:18][CH:17]=2)[N:12]=[CH:13][C:14]=1[Br:15]>O>[Br:8][C:9]1[C:10](=[O:24])[N:11]([C:16]2[CH:17]=[CH:18][C:19]([OH:22])=[CH:20][CH:21]=2)[N:12]=[CH:13][C:14]=1[Br:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344Dichloromethane2회HCID 25134Boron tribromideHCID 631734334,5-Dibromo-2-(4-methoxyphenyl)pyridazin-3(2H)-one

생성물 1

HCID 684287654,5-dibromo-2-(4-hydroxyphenyl)-2H-pyridazin-3-one수율 97.3%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A 1N dichloromethane solution (5.5 mL) of boron tribromide was added to a dichloromethane solution (30 mL) of 4,5-dibromo-2-(4-methoxyphenyl)-2H-pyridazin-3-one (1.1 g, 3.06 mmols), and stirred overnight at room temperature. Water (30 mL) was added and stirred for 30 minutes. The resulting precipitate was recovered by filtration, washed with water and chloroform and dried to provide the title compound (1.03 g, 97%).

후처리

  1. stirringstirred for 30 minutes
  2. filtrationThe resulting precipitate was recovered by filtration
  3. washwashed with water and chloroform
  4. customdried

출처 및 근거

ORD 기록
ord-3d9d0cf7ddde471781a2540f0cc9ffef
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732456B2

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