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Methyl 3-methylpyridine-2-carboxylate → (3-Methylpyridin-2-yl)methanol

HRID 2041308
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HRID 2041308 반응식
C[O:2][C:3]([C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][N:6]=1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[OH:2][CH2:3][C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][N:6]=1
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참가 물질

4

반응물 2

HCID 12264487Methyl 3-methylpyridine-2-carboxylateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 1514369(3-Methylpyridin-2-yl)methanol수율 18%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

Heat a mixture of 3-methylpicolinic acid (1.0 g, 7.3 mmol), potassium carbonate (4.1 g, 29.7 mmol), and iodomethane (4.4 g, 31.0 mmol) in acetone (35 mL) overnight under reflux. Filter, wash the residue with EtOAc, and concentrate in vacuo. Pass through a short plug of silica gel eluting with hexane/EtOAc (1:1) to provide 2-methoxycarbonyl-3-methylpyridine as a pale yellow liquid (630 mg, 57%). To a solution of 2-methoxycarbonyl-3-methylpyridine in anhydrous THF (10 mL) at 0° C., add with stirring a solution of 1M lithium aluminum hydride in THF (5 mL, 5 mmol), and continue stirring for 30 min at 0° C. Allow the mixture to warm to ambient temperature and quench cautiously with 0.5M aqueous NaOH. Heat the mixture at 60° C. for 40 min, cool to ambient temperature, extract with EtOAc, dry over anhydrous Na2SO4 and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (4:3) to give the desired intermediate (90 mg, 18%).

후처리

  1. temperatureAllow the mixture to warm to ambient temperature
  2. customquench cautiously with 0.5M aqueous NaOH
  3. temperatureHeat the mixture at 60° C. for 40 min
  4. temperaturecool to ambient temperature
  5. extractionextract with EtOAc
  6. dry with materialdry over anhydrous Na2SO4
  7. concentrationconcentrate in vacuo
  8. customPurify by chromatography on silica gel eluting with hexane/EtOAc (4:3)

출처 및 근거

ORD 기록
ord-7f0475bfc5284d44a3b79c1731f91898
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08580780B2

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