홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Potassium Acetate → 4-(6-Oxo-1,6-dihydro-pyridazin-3-yloxy)-benzoic acid methyl ester

HRID 215837
노트
인쇄 미리보기

반응식

HRID 215837 반응식
[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[N:12]=[N:13][C:14](Cl)=[CH:15][CH:16]=2)=[CH:6][CH:5]=1.C([O-])(=[O:21])C.[K+]>C(O)(=O)C>[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[CH:16]=[CH:15][C:14](=[O:21])[NH:13][N:12]=2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 517044Potassium AcetateHCID 606748904-(6-Chloro-pyridazin-3-yloxy)-benzoic acid methyl ester

생성물 1

HCID 672971734-(6-Oxo-1,6-dihydro-pyridazin-3-yloxy)-benzoic acid methyl ester수율 75.2%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 4-(6-chloro-pyridazin-3-yloxy)-benzoic acid methyl ester (1.0 g, 3.78 mmol) from the previous step and anhydrous potassium acetate (0.526 g, 5.37 mmol) in glacial acetic acid (10 ml) was refluxed for 13 h. The volatiles were evaporated in vacuo and the residue was diluted with dichloromethane (20 ml). The separated solid was collected by filtration, washed with 50% aqueous ethanol (2×5 ml) and water (4×7 ml) and dried to provide 0.7 g (43%) of 4-(6-oxo-1,6-dihydro-pyridazin-3-yloxy)-benzoic acid methyl ester.

후처리

  1. temperaturewas refluxed for 13 h
  2. customThe volatiles were evaporated in vacuo
  3. additionthe residue was diluted with dichloromethane (20 ml)
  4. filtrationThe separated solid was collected by filtration
  5. washwashed with 50% aqueous ethanol (2×5 ml) and water (4×7 ml)
  6. customdried

출처 및 근거

ORD 기록
ord-40d6a862e36b40eab8fcda3e1585e20f
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193192B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트