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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59113생성일: 2026년 10월 23일

tert-Butyl methyl ether → Methyl 2-chloro-6-(1-ethoxyvinyl)pyrimidine-4-carboxylate

https://huagongshe.com/ko/reaction/59113

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참여 물질

역할이름HCID투입량
반응물tert-Butyl methyl etherHCID 15413—
반응물Methyl 2,4-dichloropyrimidine-6-carboxylateHCID 239689—
반응물Potassium FluorideHCID 522689—
반응물Stannane, tributyl(1-ethoxyethenyl)-HCID 619414—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Methyl 2-chloro-6-(1-ethoxyvinyl)pyrimidine-4-carboxylateHCID 11782140475%

반응 조건

온도94 °C

반응 단계

Methyl 2,6-dichloropyrimidine-4-carboxylate (8.44 g, 40.77 mmol) and bis(triphenylphosphine)-palladium(II) chloride (0.572 g, 0.82 mmol) in DMF (80 mL) was degased. Tributyl(1-ethoxy-vinyl)tin (14.46 mL, 42.81 mmol) was added under argon. The mixture was heated at 94° C. for 1 h. The mixture was poured into a solution of potassium fluoride (30 g) in water (400 mL). MTBE (300 mL) was added and the mixture was stirred for 10 min. The mixture was filtered and the filter was washed with 200 mL of MTBE. The filtrate was washed with brine (100 mL), dried over sodium sulfate and the solvents were evaporated. The residue purified by column chromatography on silica eluting with DCM to give the title compound as a solid (7.40 g, 75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09439904B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-04fc7098ba644efc9570b0c89b16e660
출처 메모uspto-grants-2016_09