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Dimethyl Sulfoxide → 2-Methoxy-6-methylpyridine-4-carbaldehyde

HRID 2079128
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HRID 2079128 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][O:12][C:13]1[CH:18]=[C:17]([CH2:19][OH:20])[CH:16]=[C:15]([CH3:21])[N:14]=1>ClCCl.O.C(N(CC)CC)C>[CH3:11][O:12][C:13]1[CH:18]=[C:17]([CH:19]=[O:20])[CH:16]=[C:15]([CH3:21])[N:14]=1
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참가 물질

7

반응물 3

HCID 679Dimethyl SulfoxideHCID 65578Oxalyl chlorideHCID 53804368(2-Methoxy-6-methylpyridin-4-yl)methanol

생성물 1

HCID 595169222-Methoxy-6-methylpyridine-4-carbaldehyde

시약·촉매·용매 3

HCID 962Water용매HCID 6344Dichloromethane용매3회
HCID 8471
Triethylamine
용매

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온도
-78 °C

실험 절차

To 50 ml of dichloromethane containing 1.67 ml of oxalyl chloride there was added dropwise 1.36 ml of DMSO at −78° C. under a nitrogen atmosphere, and the mixture was stirred at −78° C. for 30 minutes. Next, 10 ml of a dichloromethane solution containing (2-methoxy-6-methyl-pyridin-4-yl)methanol was added dropwise, and the mixture was stirred at −78° C. for 30 minutes. After then adding 6.7 ml of triethylamine to the reaction mixture over a period of 10 minutes, the mixture was stirred for 30 minutes while raising the temperature from −78° C. to room temperature. Water was added to the reaction mixture, and extraction was performed with dichloromethane. The organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (1.9 g) as a light yellow oil.

후처리

  1. additionwas added dropwise
  2. stirringthe mixture was stirred at −78° C. for 30 minutes
  3. stirringthe mixture was stirred for 30 minutes
  4. temperaturewhile raising the temperature from −78° C. to room temperature
  5. washThe organic layer was washed with saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationThe desiccating agent was filtered off
  8. concentrationthe filtrate was concentrated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography (ethyl acetate-heptane)

출처 및 근거

ORD 기록
ord-1bbd9d4bb3d24789a6c17bb3755d45e4
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928228B2

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