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HRID 1457500作成日:2026年10月26日

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

https://huagongshe.com/reaction/1457500

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物(7-Octenyl)oxiraneHCID 543758—
反応物5-Decyl-2-(4-bromophenyl) pyrimidineHCID 19694912—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物1,2-Epoxy-8-{4-(5-decylpyrimidine-2-yl) phenyl}decaneHCID 5450648858%

反応条件

温度-17 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05849217
出典データセットuspto-grants-1998_12
ORD IDord-e4aec34e966548ef9de758a830861b5b
出典メモuspto-grants-1998_12