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N-methylbenzohydrazide → 1-Methyl-3-(o-tolyl)-5-phenyl-1,2,4-triazole

HRID 1111869
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반응식

HRID 1111869 반응식
C(O[C:4]([C:6]1[C:7]([CH3:12])=[CH:8][CH:9]=[CH:10][CH:11]=1)=[NH:5])C.[CH3:13][N:14]([C:16](=O)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[NH2:15]>C(OCC)C>[CH3:13][N:14]1[C:16]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:5][C:4]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[CH3:12])=[N:15]1
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참가 물질

4

반응물 2

HCID 242395N-methylbenzohydrazideHCID 12690380Benzenecarboximidic acid, 2-methyl-, ethyl ester

생성물 1

HCID 213219391-Methyl-3-(o-tolyl)-5-phenyl-1,2,4-triazole수율 32%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A mixture of 1.14 g. of o-toluimidic acid ethyl ester, 1.14 g. of 1-methyl-1-benzoylhydrazine and 0.1 g. of o-toluimidic acid ester hydrochloride, as a catalyst, is heated at about 100° C for 3 hours under reduced pressure (about 200 mm Hg) and then at about 120° C for 5 hours. The raw material is taken up with diethyl ether and the organic solution is washed with aqueous sodium bicarbonate and then dried over Na2SO4. After evaporation of the solvent, the product is distilled at 170° C/0.1 mm Hg. Yield 32%.

후처리

  1. additionA mixture of 1.14 g
  2. washthe organic solution is washed with aqueous sodium bicarbonate
  3. dry with materialdried over Na2SO4
  4. customAfter evaporation of the solvent
  5. distillationthe product is distilled at 170° C/0.1 mm Hg

출처 및 근거

ORD 기록
ord-59a23cadf0dd4d2ebdd99e3f59debc71
출처 데이터셋
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04119635

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