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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → 2-(5-methyl-1,3,4-oxadiazol-2-yl)aniline

HRID 1729032
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인쇄 미리보기

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HRID 1729032 반응식
[C:1]12[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=1)[NH:6]C(=O)O[C:2]2=O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(O)(=O)C.[C:28]([NH:31][NH2:32])(=[O:30])[CH3:29]>C1(C)C=CC=CC=1>[NH2:6][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][C:1]=1[C:2]1[O:30][C:28]([CH3:29])=[N:31][N:32]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 6101p-Toluenesulfonic acidHCID 8359Isatoic AnhydrideHCID 14039Acetohydrazide

생성물 1

HCID 134097122-(5-methyl-1,3,4-oxadiazol-2-yl)aniline

시약·촉매·용매 1

HCID 1140Toluene용매2회

반응 조건

온도
120 °C

실험 절차

A mixture of isatoic anhydride (16.3 g, 0.1 mol), p-toluenesulfonic acid (0.2 g, 1.1 mmol), glacial acetic acid (10 ml), acethydrazide (7.4 g, 0.1 mol) and dry toluene (90 ml) was stirred at 120° C. for 4 h, cooledto room temperature and poured into ice water. Toluene (500 ml) was added, and the phases were separated. The aqueous phase was extracted with CH2Cl2 (2×100 ml).

후처리

  1. customcooledto room temperature
  2. customthe phases were separated
  3. extractionThe aqueous phase was extracted with CH2Cl2 (2×100 ml)

출처 및 근거

ORD 기록
ord-ffb816bf758d4ab3ae9d28fc55f06bf4
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05330990

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