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Potassium Carbonate → HCID 15917391, 화합물

HRID 1758142
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HRID 1758142 반응식
[Cl:1][C:2]1[CH:3]=[N:4][C:5]([O:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[OH:15])=[N:6][CH:7]=1.C(=O)([O-])[O-].[K+].[K+].Cl[C:23]1[CH:28]=[CH:27][C:26]([N+:29]([O-:31])=[O:30])=[CH:25][N:24]=1>C(C(C)=O)C>[Cl:1][C:2]1[CH:7]=[N:6][C:5]([O:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[O:15][C:23]2[CH:28]=[CH:27][C:26]([N+:29]([O-:31])=[O:30])=[CH:25][N:24]=2)=[N:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 783082-Chloro-5-nitropyridineHCID 15917392HCID 15917392, 화합물

생성물 1

HCID 15917391HCID 15917391, 화합물수율 99.6%

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

After heating at reflux a mixture of 1.5 grams (0.0067 mole) 2-(5-chloropyrimidin-2-yloxy)phenol, 1.2 grams potassium carbonate, 1.3 grams 2-chloro-5-nitropyridine and 40 ml of methyl ethyl ketone, the reaction mixture was poured into excess H2 0 and the aqueous mixture extracted with ethyl ether (200 ml). The ether layer was washed with saturated NaHCO3, H2O, brine, dried (MgSO4), filtered, and evaporated to yield 2.3 grams of a yellow-orange oil which was purified by silica gel column chromatography (CH2Cl2 as the eluent). NMR (CDCl3): δ6.90 (d, 1H, pyridine ring proton), 7.35 (s, 4H, ArH), 8.25-8.50 (m, 1H, pyridine ring proton), 8.45 (s, 2H, pyrimidine ring protons), 8.95 (d, 1H, pyridine ring proton).

후처리

  1. temperatureAfter heating
  2. temperatureat reflux
  3. additionthe reaction mixture was poured into excess H2 0
  4. extractionthe aqueous mixture extracted with ethyl ether (200 ml)
  5. washThe ether layer was washed with saturated NaHCO3, H2O, brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-81063725072944429c8078058b7b7030
출처 데이터셋
uspto-grants-1983_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04371736

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