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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1457500생성일: 2026년 10월 26일

Potassium Carbonate → 1,2-Epoxy-8-{4-(5-decylpyrimidine-2-yl) phenyl}decane

https://huagongshe.com/reaction/1457500

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물9-Borabicyclo(3.3.1)nonaneHCID 78966—
반응물(7-Octenyl)oxiraneHCID 543758—
반응물5-Decyl-2-(4-bromophenyl) pyrimidineHCID 19694912—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물1,2-Epoxy-8-{4-(5-decylpyrimidine-2-yl) phenyl}decaneHCID 5450648858%

반응 조건

온도-17 °C

반응 단계

1.36 g (8.8 mmol) of optically active 1,2-epoxy-9-decene and 6 ml of THF were injected, and they were cooled to -17° C. Then, 9-borabicyclo [3.3.1]nonane (0.5M THF solution) was dripped, and stirring at 0° C. was performed for one hour. Then, stirring at room temperature was performed for one hour, and then 0.26 g (0.073 mmol) of tetrakis (triphenylphosphine) palladium, 3.00 g (8.00 mmol) of 5-decyl-2-(4-bromophenyl) pyrimidine, 10 ml of DMF, and 2.21 g (16.0 mmol) of potassium carbonate were added, and stirring at 60° C. was performed for 5 hours. After reactions had been completed, water was added, and extraction with ethyl acetate was performed. The extracted solution was dried, and then the solvent was removed by filtration. Then, refining was performed with a silica gel column chromatography (developing solvent: toluene/ethyl acetate=50/1) and by recrystallization (toluene/methanol) so that 2.10 g of 1,2-epoxy-8-{4-(5-decylpyrimidine-2-yl) phenyl}decane was obtained (yield 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05849217
출처 데이터셋uspto-grants-1998_12
ORD IDord-e4aec34e966548ef9de758a830861b5b
출처 메모uspto-grants-1998_12