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Isobutanol → HCID 61375113, 화합물

HRID 1620324
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HRID 1620324 반응식
[CH3:1][CH:2]([CH3:5])[CH2:3][OH:4].[H-].[Na+].[Br:8][C:9]1[CH:10]=[CH:11][C:12](F)=[N:13][CH:14]=1>CN(C=O)C.O>[Br:8][C:9]1[CH:10]=[CH:11][C:12]([O:4][CH2:3][CH:2]([CH3:5])[CH3:1])=[N:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6560IsobutanolHCID 24758Sodium hydrideHCID 27831685-Bromo-2-fluoropyridine

생성물 1

HCID 61375113HCID 61375113, 화합물수율 86.3%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

To 2-methyl-propan-1-ol (10 g, 0.41 mol) was added NaH (60%, 8.2 g, 0.204 mol) portionwise under a nitrogen atmosphere at room temperature over 10 minutes. The mixture was refluxed for 30 minutes. A solution of 5-bromo-2-fluoro-pyridine (24 g, 0.136 mol) in DMF (400 mL) was added dropwise and the mixture refluxed for 18 hours. The reaction mixture was then diluted with water (1 L) and extracted with EtOAc (3×500 mL). The combined organics were washed with brine (3×300 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The crude residue obtained was purified by flash column chromatography eluting with petroleum ether to yield the title compound as a colourless oil (27 g).

후처리

  1. temperatureThe mixture was refluxed for 30 minutes
  2. temperaturethe mixture refluxed for 18 hours
  3. extractionextracted with EtOAc (3×500 mL)
  4. washThe combined organics were washed with brine (3×300 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude residue obtained
  9. customwas purified by flash column chromatography
  10. washeluting with petroleum ether

출처 및 근거

ORD 기록
ord-6ef68ccd4d204eae9af74f18bff5f832
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772343B2

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