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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl iodide → 1H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-phenyl-

HRID 257167
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HRID 257167 반응식
[CH3:1][N:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:5][NH:4][C:3]1=[S:13].[OH-].[Na+].[CH3:16]I>C(O)C>[CH3:1][N:2]1[C:3]([S:13][CH3:16])=[N:4][N:5]=[C:6]1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 14798Sodium HydroxideHCID 7197994-methyl-5-phenyl-4H-1,2,4-triazole-3-thiol

생성물 1

HCID 2132261H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-phenyl-

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a stirred solution of 4-methyl-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione (5.0 g, 2.6×10-2 mole) and 1 molar aqueous NaOH (59 ml, 5.9×10-2 mole) was added a solution of methyl iodide (2.6 ml, 4.2×10-2 mole) and ethanol (13 ml). The reaction was stirred for 3 hours and it was then placed in the refrigerator. After standing in the refrigerator overnight, the precipitate was collected by filtration. Crystallization from isopropanol afforded colorless needles, Mp 134°-135° C.

후처리

  1. customAfter standing in the refrigerator overnight
  2. filtrationthe precipitate was collected by filtration
  3. customCrystallization from isopropanol afforded colorless needles, Mp 134°-135° C.

출처 및 근거

ORD 기록
ord-ce017cddd595464fa098e311bfd23611
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05260450

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