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4-Acetylpyridine → Phenyl [1-(4-pyridinyl)ethylidene]carbazate monohydrochloride

HRID 1085953
노트
인쇄 미리보기

반응식

HRID 1085953 반응식
[C:1]([C:4]1[CH:9]=[CH:8][N:7]=[CH:6][CH:5]=1)(=O)[CH3:2].[ClH:10].[C:11]([O:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)(=[O:14])[NH:12][NH2:13]>C(O)C>[ClH:10].[N:7]1[CH:8]=[CH:9][C:4]([C:1](=[N:13][NH:12][C:11]([O:15][C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)=[O:14])[CH3:2])=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 142824-AcetylpyridineHCID 19830215Phenyl carbazate hydrochloride

생성물 1

HCID 86744746Phenyl [1-(4-pyridinyl)ethylidene]carbazate monohydrochloride수율 97%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 12.11 gm (0.1 mole) of 4-acetylpyridine, 18.85 gm (0.1 mole) of phenyl carbazate hydrochloride and 250 ml of absolute ethanol is refluxed 6 hr and cooled. The reaction mixture is evaporated to dryness in vacuo to give a rose-colored solid. The crude product is crystallized from absolute ethanol to yield 28.13 gm (97%) of the title compound having a melting point of 159.1° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperatureis refluxed 6 hr
  2. temperaturecooled
  3. customThe reaction mixture is evaporated to dryness in vacuo
  4. customto give a rose-colored solid
  5. customThe crude product is crystallized from absolute ethanol

출처 및 근거

ORD 기록
ord-3f338981cf634822b7248b2d59c67868
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05011932

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