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Potassium Carbonate → HCID 86762491, 화합물

HRID 1618905
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HRID 1618905 반응식
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([OH:12])=[CH:7]2.C(=O)([O-])[O-].[K+].[K+].C[C:20]([C:22]1[C:27]([F:28])=[CH:26][CH:25]=[CH:24][C:23]=1F)=[O:21]>C(#N)C>[F:28][C:27]1[CH:26]=[CH:25][CH:24]=[C:23]([O:12][C:8]2[CH:9]=[N:10][C:11]3[C:6]([CH:7]=2)=[CH:5][CH:4]=[CH:3][C:2]=3[F:1])[C:22]=1[CH:20]=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 836431-(2,6-Difluorophenyl)ethan-1-oneHCID 682880678-fluoroquinolin-3-ol

생성물 1

HCID 86762491HCID 86762491, 화합물수율 57.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

After 30 ml of acetonitrile was added to 3.0 g of 8-fluoro-3-hydroxyquinoline, 3.1 g of potassium carbonate and 3.5 g of 2,6-difluoroacetophenone were added. After the reaction solution was heated under reflux for 3 hours, the reaction solution was filtered with CELITE. After the filtrate was extracted with ethyl acetate, the organic layer was concentrated and purified by silica gel column chromatography to obtain 3.0 g of 2-fluoro-6-(8-fluoroquinolin-3-yloxy)-benzaldehyde (Compound Number 341).

후처리

  1. additionwere added
  2. temperatureAfter the reaction solution was heated
  3. temperatureunder reflux for 3 hours
  4. filtrationthe reaction solution was filtered with CELITE
  5. extractionAfter the filtrate was extracted with ethyl acetate
  6. concentrationthe organic layer was concentrated
  7. custompurified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-7978b09554d24f46b7bef5e1a2d6734c
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772200B2

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