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

HRID 2080368
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HRID 2080368 반응식
C([Li])(C)(C)C.CCCCC.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][N:13]=1.[N:19]1[CH:24]=[CH:23][C:22]([CH:25]=[O:26])=[CH:21][CH:20]=1>CO.O.CCOCC>[Cl:18][C:15]1[C:14]([CH:25]([C:22]2[CH:23]=[CH:24][N:19]=[CH:20][CH:21]=2)[OH:26])=[N:13][C:12]([Cl:11])=[CH:17][CH:16]=1
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참가 물질

8

반응물 4

HCID 8003PentaneHCID 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 3

HCID 887Methanol용매
HCID 962
Water
용매
HCID 3283Diethyl Ether용매

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온도
-78 °C

실험 절차

Under stirring at −78° C., t-butyl lithium (a 1.51M pentane solution: 4.6 ml) was added dropwise to an ether (20 ml) solution of 2,5-dichloropyridine (1.02 g, 6.89 mmol). After stirring at −78° C. for 2 hours, pyridine-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 then added to the reaction mixture. The temperature of the resulting mixture was raised to room temperature. The mixture was extracted with methylene chloride. The extract was then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography. The fraction obtained from the methanol:methylene chloride (=1:50) eluate was concentrated under reduced pressure. The solid thus obtained was washed with ether and then collected by filtration to give the title compound (819 mg, 3.21 mmol, 47%) 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 of the resulting mixture was raised to room temperature
  4. extractionThe mixture was extracted with methylene chloride
  5. dry with materialThe extract was then dried over anhydrous sodium sulfate
  6. filtrationAfter filtration
  7. concentrationthe filtrate was concentrated under reduced pressure
  8. customThe residue thus obtained
  9. concentrationmethylene chloride (=1:50) eluate was concentrated under reduced pressure
  10. customThe solid thus obtained
  11. washwas washed with ether
  12. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-2f691215afbb4c47bf1848c798865817
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932271B2

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