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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Potassium Carbonate → HCID 13023013, 화합물

HRID 1759361
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인쇄 미리보기

반응식

HRID 1759361 반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[OH:14])=[CH:6][CH:7]=1.[CH2:15]([CH:17]1[O:19][CH2:18]1)Br.C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[Cl:1][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH2:15][CH:17]2[O:19][CH2:18]2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 18430EpibromohydrinHCID 30187332-(6-Chloro-3-pyridazinyl)phenol

생성물 1

HCID 13023013HCID 13023013, 화합물

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

A mixture of 3-chloro-6-(2-hydroxyphenyl)pyridazine (2.69 g.), epibromohydrin (4.5 ml.), anhydrous potassium carbonate (3.6 g.) and dry butane-2-one (100 ml.) was stirred and heated under reflux for 16 hours. The mixture was filtered and the filtrate was evaporated to dryness and the residue was twice recrystallized from ethanol to give 3-chloro-6-(2-epoxypropoxyphenyl)pyridazine, m.p. 118°-119°.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 16 hours
  3. filtrationThe mixture was filtered
  4. customthe filtrate was evaporated to dryness
  5. customthe residue was twice recrystallized from ethanol

출처 및 근거

ORD 기록
ord-c7673871e70141e88e1fed2644ed4017
출처 데이터셋
uspto-grants-1982_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04340733

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