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Water → (3,6-Dichloropyridin-2-yl) (pyridine-4-yl)methanol

HRID 748862
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HRID 748862 반응식
C([Li])(C)(C)C.[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][N:8]=1.[N:14]1[CH:19]=[CH:18][C:17]([CH:20]=[O:21])=[CH:16][CH:15]=1.O>CCOCC.CO.C(Cl)Cl>[Cl:13][C:10]1[C:9]([CH:20]([C:17]2[CH:18]=[CH:19][N:14]=[CH:15][CH:16]=2)[OH:21])=[N:8][C:7]([Cl:6])=[CH:12][CH:11]=1
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참가 물질

7

반응물 4

HCID 962WaterHCID 133894-PyridinecarboxaldehydeHCID 276852,5-DichloropyridineHCID 178418306HCID 178418306, 화합물

생성물 1

HCID 23028600(3,6-Dichloropyridin-2-yl) (pyridine-4-yl)methanol수율 47%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 21226129
Dichloromethane methanol
용매

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온도
-78 °C

실험 절차

Under stirring at −78° C., tert-butyl lithium (1.51M pentane solution: 4.6 ml) was added dropwise to a solution of 2,5-dichloropyridine (1.02 g, 6.89 mmol) in ether (20 ml). After stirring at −78° C. for 2 hours, pyridin-4-carbaldehyde (0.65 ml, 6.89 mmol) was added to the reaction mixture. The resulting mixture was stirred at −78° C. for 1 hour. Water was added to the reaction mixture and the temperature was raised to room temperature. The mixture was extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate and filtered. The filtrate was then concentrated under reduced pressure. The residue thus obtained was subjected to chromatography on a silica gel column. A fraction obtained from the eluate with methanol:methylene chloride (1:50) was concentrated under reduced pressure. The solid thus obtained was washed with ether and collected by filtration, whereby the title compound (819 mg, 3.21 mmol, 47%) was obtained as a white powder.

후처리

  1. stirringAfter stirring at −78° C. for 2 hours
  2. stirringThe resulting mixture was stirred at −78° C. for 1 hour
  3. temperaturethe temperature was raised to room temperature
  4. extractionThe mixture was extracted with methylene chloride
  5. dry with materialThe extract was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was then concentrated under reduced pressure
  8. customThe residue thus obtained
  9. concentrationwas concentrated under reduced pressure
  10. customThe solid thus obtained
  11. washwas washed with ether

출처 및 근거

ORD 기록
ord-b79583c4ea4f4da8830594ad67b8bf8b
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07399775B2

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