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2-Methylbenzenesulfonic acid → HCID 86738432, 화합물

HRID 1649081
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HRID 1649081 반응식
[C:1]([C:4]1[C:5]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[N:6][O:7][C:8]=1[CH3:9])(=O)[CH3:2].[C:16]1([NH:22][NH2:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C1(C)C(S(O)(=O)=O)=CC=CC=1>C(O)C>[C:16]1([NH:22][N:23]=[C:1]([C:4]2[C:5]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[N:6][O:7][C:8]=2[CH3:9])[CH3:2])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 69252-Methylbenzenesulfonic acidHCID 7516PhenylhydrazineHCID 3185241-(5-Methyl-3-phenylisoxazol-4-yl)ethanone

생성물 1

HCID 86738432HCID 86738432, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 80.4 g. (0.4 mole) of 4-acetyl-5-methyl-3-phenyl isoxazole, 39.4 ml. (0.4 mole) of phenyl hydrazine and 500 mg. toluenesulfonic acid in 400 ml. ethanol is stirred at room temperature for 48 hours. The resulting solid is filtered and washed with cold ether to give 1-(5-methyl-3-phenyl-4-isoxazolyl)-1-ethanone phenyl hydrazone; m.p. 129°-133°0 C.

후처리

  1. additionA mixture of 80.4 g
  2. filtrationThe resulting solid is filtered
  3. washwashed with cold ether

출처 및 근거

ORD 기록
ord-ddba2f609e26433ba82155e5c44325ff
출처 데이터셋
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04415568

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