Ethyl Acetate → 2-(2-Phenyl-1,3-thiazol-4-yl)acetonitrile

HRID 1107683

반응식

HRID 1107683 반응식
Cl[CH2:2][C:3]1[N:4]=[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[S:6][CH:7]=1.[C-:14]#[N:15].[K+].C(OCC)(=O)C>C(#N)C.C1OCCOC2C(=CC=CC=2)OCCOCCOC2C(=CC=CC=2)OC1>[C:14]([CH2:2][C:3]1[N:4]=[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[S:6][CH:7]=1)#[N:15]

참가 물질

6

반응물 3

HCID 8857Ethyl AcetateHCID 9032Potassium CyanideHCID 2369694-(Chloromethyl)-2-phenyl-1,3-thiazole

생성물 1

HCID 2238442-(2-Phenyl-1,3-thiazol-4-yl)acetonitrile수율 73.8%

시약·촉매·용매 2

HCID 26541Dibenzo-18-crown-6촉매HCID 6342Acetonitrile용매

실험 절차

1.39 g of 4-chloromethyl-2-phenylthiazole was dissolved in 10 ml of acetonitrile, and 0.65 g of potassium cyanide and 0.05 g of dibenzo-18-crown-6-ether were added thereto at room temperature, and then heated under reflux for 10 hours. After the temperature was returned to room temperature, ethyl acetate was added the resulting mixture, and the insoluble solid was removed through filtration. The resulting ethyl acetate solution was washed with saturated saline and water, and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residual product was purified through silica gel column chromatography to obtain 0.98 g of 4-cyanomethyl-2-phenylthiazole from the fraction eluted with chloroform.

후처리

  1. temperatureunder reflux for 10 hours
  2. customwas returned to room temperature
  3. customthe insoluble solid was removed through filtration
  4. washThe resulting ethyl acetate solution was washed with saturated saline and water
  5. dry with materialdried over sodium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe residual product was purified through silica gel column chromatography

출처 및 근거

ORD 기록
ord-32f4df3f19f8454aaaa41e0ff4865b6c
출처 데이터셋
uspto-grants-2000_05
특허 번호
US06063734

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