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Bis(4-nitrophenyl)methanone → n-Hydroxy-1,1-bis(4-nitrophenyl)methanimine

HRID 376795
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인쇄 미리보기

반응식

HRID 376795 반응식
Cl.[NH2:2][OH:3].[N+:4]([C:7]1[CH:23]=[CH:22][C:10]([C:11]([C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=2)=O)=[CH:9][CH:8]=1)([O-:6])=[O:5]>C(O)C>[N+:4]([C:7]1[CH:23]=[CH:22][C:10]([C:11](=[N:2][OH:3])[C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-:21])=[O:20])=[CH:15][CH:14]=2)=[CH:9][CH:8]=1)([O-:6])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 245528Bis(4-nitrophenyl)methanoneHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 289708n-Hydroxy-1,1-bis(4-nitrophenyl)methanimine수율 70%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of hydroxylamine hydrochloride (10.2 g, 147 mmol) was added to a suspension of 4,4'-dinitrobenzophenone (19 g, 70 mmol) in 100 ml of ethanol. The reaction mixture was heated to reflux for 2 hours, cooled to room temperature, and the solid collected by filtration. Recrystallization from ethanol provided the title compound (14.0 g, 70%) as pale yellow crystals. mp 194° C.;

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 2 hours
  3. filtrationthe solid collected by filtration
  4. customRecrystallization from ethanol

출처 및 근거

ORD 기록
ord-4af6ddbae74f430e8c94b2ee2148f6d0
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06022523

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