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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1742608생성일: 2026년 10월 25일

Dimethylformamide → 4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)-methoxy]-2-pyrimidinecarbonitrile

https://huagongshe.com/reaction/1742608

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물PyrimidineHCID 9260—
반응물Oxalyl chlorideHCID 65578—
반응물4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidinecarboxaldehyde oximeHCID 136378412—
용매AcetonitrileHCID 6342—
생성물4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)-methoxy]-2-pyrimidinecarbonitrileHCID 1992298622.3%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05340815
출처 데이터셋uspto-grants-1994_08
ORD IDord-1e6b7d209bd24b1fb2b70f7811b85fe9
출처 메모uspto-grants-1994_08