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Sodium Cyanide → (6-Methoxypyridin-3-yl)acetonitrile

HRID 1896245
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HRID 1896245 반응식
[C-:1]#[N:2].[Na+].Cl[CH2:5][C:6]1[CH:7]=[CH:8][C:9]([O:12][CH3:13])=[N:10][CH:11]=1>CS(C)=O.[Cl-].[Na+].O>[CH3:13][O:12][C:9]1[N:10]=[CH:11][C:6]([CH2:5][C:1]#[N:2])=[CH:7][CH:8]=1
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참가 물질

5

반응물 2

HCID 8929Sodium CyanideHCID 137528915-(Chloromethyl)-2-methoxypyridine

생성물 1

HCID 45079846(6-Methoxypyridin-3-yl)acetonitrile수율 63.9%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 57417360Sodium chloride; water용매

실험 절차

Sodium cyanide (1.25 g, 25.4 mmol) was added to a solution of 5-(chloromethyl)-2-methoxypyridine (1.00 g, 6.34 mmol) in DMSO (10 ml) and stirred for 18 h at room temperature. After completion of reaction, the reaction mixture was diluted with brine and the compound was extracted with DCM (3×35 ml). The combined organic layers were dried over anhydrous sodium sulfate, filtered and evaporated. The crude compound was purified by column chromatography using 100-200 silica gel, 10% ethyl acetate in petroleum ether as eluent to afford 0.6 g (63.8%) of 2-(6-methoxypyridin-3-yl)acetonitrile as white color solid.

후처리

  1. customAfter completion of reaction
  2. extractionthe compound was extracted with DCM (3×35 ml)
  3. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customThe crude compound was purified by column chromatography

출처 및 근거

ORD 기록
ord-7c2a6a92ed3944848e74570f3cbf7533
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08518948B2

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