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Ammonium Hydroxide → 5-methyl-6-phenyl-3(2H)-Pyridazinone

HRID 372711
노트
인쇄 미리보기

반응식

HRID 372711 반응식
[CH3:1][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][C:11](Br)=[CH:10][CH:9]=2)=[N:6][NH:5][C:4](=[O:15])[CH:3]=1.[OH-].[NH4+].[H][H]>[Pd].C(O)C>[CH3:1][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][NH:5][C:4](=[O:15])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 14923Ammonium HydroxideHCID 233336686-(p-bromophenyl)-5-methyl-3(2H)-pyridazinoneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 27838415-methyl-6-phenyl-3(2H)-Pyridazinone

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

반응 조건

온도
50 °C

실험 절차

A 10.0 g. portion of 5-methyl-6-p-bromophenyl-3(2H)-pyridazinone and 1.0 g. of 10% palladium on carbon catalyst in 150 ml. of ethanol and 50 ml. of ammonium hydroxide is shaken under 40 lb. of hydrogen pressure for 4 hours in a Parr bottle, heated to 50° C. with an outside jacket. The reaction mixture is suction filtered and the filtrate concentrated to a white solid which is washed with water and air dried to afford 5-methyl-6-phenyl-3(2H)-pyridazinone as white crystals.

후처리

  1. filtrationfiltered
  2. concentrationthe filtrate concentrated to a white solid which
  3. washis washed with water and air
  4. customdried

출처 및 근거

ORD 기록
ord-d49d3470fa454469ba9a7803968e1111
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04092311

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