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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1742771생성일: 2026년 10월 25일

Acetic Acid → HCID 178446993, 화합물

https://huagongshe.com/reaction/1742771

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물DiisopropylamineHCID 7912—
반응물4-Chloro-6-(3-methylbut-1-oxy)-2-phenylpyrimidineHCID 19006799—
반응물Titanocene dichiorideHCID 124040768—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물HCID 178446993HCID 178446993—

반응 조건

온도-70 °C

반응 단계

69 ml (0.11 mol, 1.6M) of butyllithium are added dropwise over the course of 15 minutes under a nitrogen atmosphere to a solution of 15.6 ml (0.11 mol) of diisopropylamine in 200 ml of tetrahydrofuran at 0° C. This solution is added dropwise at from -70° to -60° C. over the course of 2 hours to a suspension of 24.9 g (0.1 mol) of titanocene dichloride and 27.7 g (0.1 mol) of 4-chloro-6-(3-methylbut-1-oxy)-2-phenylpyrimidine in 1000 ml of tetrahydrofuran. The reaction mixture is stirred at -70° C. for 1 hour, allowed to warm to room temperature over the course of about 3 hours and then poured, with stirring, into water and 19.0 g (0.23 mol) of acetic acid. The resultant red-orange emulsion is filtered through ®Hyflo. The organic phase is separated off, dried using magnesium sulfate, filtered and evaporated on a rotary evaporator. The residue is purified by flash chromatography with hexane:ethyl acetate in the ratio 3:1 as eluent, giving 11.2 g (22.4% of theory) of the title compound as a yellow powder having a melting point of 158° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05340701
출처 데이터셋uspto-grants-1994_08
ORD IDord-12502a90446245439539eafe2e1e56e7
출처 메모uspto-grants-1994_08