Sodium Cyanide → 2-(2-tert-Butyl-1,3-oxazol-4-yl)acetonitrile

HRID 990736노트

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HRID 990736 반응식
[C-:1]#[N:2].[Na+].[C:4]([C:8]1[O:9][CH:10]=[C:11]([CH2:13]Cl)[N:12]=1)([CH3:7])([CH3:6])[CH3:5].[OH-].[Na+]>CS(C)=O>[C:4]([C:8]1[O:9][CH:10]=[C:11]([CH2:13][C:1]#[N:2])[N:12]=1)([CH3:7])([CH3:6])[CH3:5]

참가 물질

5

반응물 3

HCID 8929Sodium CyanideHCID 14798Sodium HydroxideHCID 221695102-tert-Butyl-4-(chloromethyl)-1,3-oxazole

생성물 1

HCID 221695172-(2-tert-Butyl-1,3-oxazol-4-yl)acetonitrile수율 92.6%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

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온도
65 °C

실험 절차

6.2 g of sodium cyanide was weighed, 50 ml of dimethylsulfoxide was added thereto, and a dimethylsulfoxide solution of 16.9 g of 2-tert-butyl-4-chloromethyloxazole was dropwise added thereto, and heated on an oil bath at 65° C. for 1 hour with stirring. After the resulting product was cooled to room temperature, 150 ml of a dilute aqueous solution of sodium hydroxide was added thereto, and extracted with toluene. The organic layer was fully washed with water, and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 14.8 g of 2-tert-butyl-4-cyanomethyloxazole.

후처리

  1. temperatureAfter the resulting product was cooled to room temperature
  2. extractionextracted with toluene
  3. washThe organic layer was fully washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-d5b1e36f55af4eb4a4a000b4a065e621
출처 데이터셋
uspto-grants-2002_10
특허 번호
US06462049B1

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