반응식
CN(C)C=O.C(Cl)(=O)C(Cl)=O.[CH3:12][C:13]([C:16]1[C:21]([O:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH3:28])=[C:20]([C:29]([CH3:32])([CH3:31])[CH3:30])[N:19]=[C:18]([CH:33]=[N:34]O)[N:17]=1)([CH3:15])[CH3:14].N1C=CC=NC=1>C(#N)C>[CH3:15][C:13]([C:16]1[C:21]([O:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH3:28])=[C:20]([C:29]([CH3:32])([CH3:31])[CH3:30])[N:19]=[C:18]([C:33]#[N:34])[N:17]=1)([CH3:12])[CH3:14]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 0 °C
실험 절차
Dimethylformamide (0.05 g, 0.6 mmoles) is cooled to 0° C. in 10 mL of acetonitrile under argon. Oxalyl chloride (0.1 g, 0.9 mmoles) is added and the reaction mixture is stirred at 0° C. for 10 minutes. 4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidinecarboxaldehyde oxime (0.2 g, 0.6 mmoles) is dissolved in 10 mL of acetonitrile and cooled to 0° C. The vilsmier reagent prepared above is added to the pyrimidine solution at 0° C. After 3 hours at 0° C, the reaction is quenched by the addition of 10 mL of saturated sodium bicarbonate and extracted with ether (3×10 mL). The organic extract is washed with 50 mL of brine and dried over magnesium sulfate. Evaporation of the solvent gives a red oil which is purified by flash chromatography (silica, 10% ether/chloroform) to give 4,6-bis (1,1-dimethylethyl) -5-[(2-methoxyethoxy)methoxy]-2-pyrimidinecarbonitrile (43 mg, 22%) as an oil.
후처리
- temperaturecooled to 0° C
- customThe vilsmier reagent prepared
- waitAfter 3 hours at 0° C
- customthe reaction is quenched by the addition of 10 mL of saturated sodium bicarbonate
- extractionextracted with ether (3×10 mL)
- extractionThe organic extract
- washis washed with 50 mL of brine
- dry with materialdried over magnesium sulfate
- customEvaporation of the solvent
- customgives a red oil which
- customis purified by flash chromatography (silica, 10% ether/chloroform)
출처 및 근거
- ORD 기록
- ord-1e6b7d209bd24b1fb2b70f7811b85fe9
- 출처 데이터셋
- uspto-grants-1994_08
- 특허 번호
- US05340815
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