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5-Chloro-8-hydroxyquinoline → 8-(2-Hydroxyethyl)5-chloroquinoline

HRID 1025536
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HRID 1025536 반응식
[Cl:1][C:2]1[CH:11]=[CH:10][C:9](O)=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.C1(=O)O[CH2:16][CH2:15][O:14]1.C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C>[OH:14][CH2:15][CH2:16][C:9]1[CH:10]=[CH:11][C:2]([Cl:1])=[C:3]2[C:8]=1[N:7]=[CH:6][CH:5]=[CH:4]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 28175-Chloro-8-hydroxyquinolineHCID 7303Ethylene carbonateHCID 10796Cesium carbonate

생성물 1

HCID 452801778-(2-Hydroxyethyl)5-chloroquinoline

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

A mixture of 5-chloro-8-hydroxyquinoline (1 mmol, 180 mg), ethylene carbonate (2 mmol, 180 mg) and Cs2CO3 (0.6 mmol, 195 mg) in dry DMF (10 mL) was stirred vigorously at 120° C. for 3 h. DMF was evaporated under high-vacuum and the residue was dissolved in water (15 mL), extracted twice with dichloromethane (15 mL), and the residue left after evaporation of dichloromethane was chromatographed over silica gel (eluent: 4:1 hexanes-EtOAc). A biege colored solid was obtained (174 mg, 78%).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customDMF was evaporated under high-vacuum
  2. dissolutionthe residue was dissolved in water (15 mL)
  3. extractionextracted twice with dichloromethane (15 mL)
  4. waitthe residue left
  5. customafter evaporation of dichloromethane
  6. customwas chromatographed over silica gel (eluent: 4:1 hexanes-EtOAc)
  7. customwas obtained (174 mg, 78%)

출처 및 근거

ORD 기록
ord-fa988a59dc914388a1cf80dbb5cb3d0e
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729097B2

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