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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6342생성일: 2026년 10월 24일

Sodium hydride → 4,6-Ditert-butyl-5-[(2-methoxyethoxy)methoxy]-2-methylpyrimidine

https://huagongshe.com/ko/reaction/6342

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
반응물4,6-Bis(1,1-dimethylethyl)-5-hydroxy 2-methylpyrimidineHCID 9877866—
용매TetrahydrofuranHCID 8028—
생성물4,6-Ditert-butyl-5-[(2-methoxyethoxy)methoxy]-2-methylpyrimidineHCID 19922990—

반응 단계

4,6-Bis(1,1-dimethylethyl) 5 hydroxy-2-methyl pyrimidine (9.8 g, 44.1 mmoles) is dissolved in 100 mL of tetrahydrofuran and added dropwise to a suspension of sodium hydride (1.2 g, 48.5 mmoles) in THF (50 mL) at 0° C. The reaction mixture is warmed to room temperature over 15 minutes. 2-Methoxyethoxymethyl chloride (7.1 g, 57.3 mmoles) is added to the reaction mixture at room temperature. After being stirred at room temperature for 4 hours, the reaction is quenched by the addition of saturated ammonium chloride and the tetrahydrofuran is evaporated. The organics are extracted into 300 mL of ether. The ether is washed with 100 mL of brine and dried over magnesium sulfate. Evaporation of the solvent gives the crude product which is purified by flash chromatography (silica, 10% ether/hexane). Yield of 4,6 bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-methylpyrimidine=11.3 g (82%) as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248682
출처 데이터셋uspto-grants-1993_09
ORD IDord-9502ecdb7f4d41659d2e170dd6a9e06b
출처 메모uspto-grants-1993_09