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Hydrochloric Acid → 1-Methyl-3-phenyl-5-(2-hydroxymethylphenyl)-1,2,4-triazole

HRID 26645
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인쇄 미리보기

반응식

HRID 26645 반응식
[CH:1](=[N:8][N:9]([C:11]1[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[CH2:14][O:13][N:12]=1)[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>C(O)C>[OH:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[C:11]1[N:9]([CH3:10])[N:8]=[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[N:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 54035358HCID 54035358, 화합물

생성물 1

HCID 218245361-Methyl-3-phenyl-5-(2-hydroxymethylphenyl)-1,2,4-triazole수율 96%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

A suspension of 1.2 g. of 4-(2-benzylidene-1-methylhydrazino)-1H-2,3-benzoxazine in 12 ml. of ethanol and 12 ml. of aqueous 5% HCl is heated on a water bath for three hours. The ethanol is removed by distillation and the residue, neutralized with aqueous NaHCO3, is cooled to about 0° C. The precipitate is filtered and crystallized from ethanol. M.p. 122° C. Yield 96%.

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후처리

  1. additionA suspension of 1.2 g
  2. customThe ethanol is removed by distillation
  3. filtrationThe precipitate is filtered
  4. customcrystallized from ethanol

출처 및 근거

ORD 기록
ord-0190eedbcd6c47649bc7d515f04522ff
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04151169

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