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HRID 1736477作成日:2026年10月26日

1,2-Bis(diphenylphosphino)ethane → (Cyclopent-2-en-1-yl)benzene

https://huagongshe.com/reaction/1736477

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Bis(diphenylphosphino)ethaneHCID 74267—
反応物Acetic acid, cyclopent-2-en-1-yl esterHCID 140735—
反応物HCID 178418255HCID 178418255—
触媒1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
触媒ZincchlorideHCID 3007855—
溶媒TetrahydrofuranHCID 8028—
生成物(Cyclopent-2-en-1-yl)benzeneHCID 142190—

反応条件

温度40 °C

反応手順

A solution of 8 mL of 2M phenylmagnesium bromide in THF was added dropwise to a solution of 32.2 mL (0.016 mole) of 0.5M zinc chloride in THF. A solution of 3.05g (0.024 mole) of 3-acetoxycyclopent-1-ene in 25 mL of dry THF was added, and 321 mg of 1,2-bis(diphenylphosphino)ethane and 462 mg of palladium bis(dibenzylideneacetone) added. The reaction mixture was heated at 40° C. for 18h. The reaction was cooled to room temperature and the solids filtered off. Ether was added, and the organic layer was washed sequentially with saturated ammonium chloride, water, and brine. After drying (MgSO4), the solvent was evaporated in vacuo to give 6 g of a yellow oil. Flash chromatography (SiO2) eluting with hexane gave 760 mg of an oil. Mass spectrum (Cl-NH3) m/z=145 (M+1); 300 MHz NMR (CDCl3) δ 1.68-1.78 (m, 1H); 2.32-2.6 (m, 3H); 3.85-3.96 (m, 1H); 5.72-5.82 (m, 1H); 5.92-6.01 (m, 1H); 7.12-7.38 (m, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05541217
出典データセットuspto-grants-1996_07
ORD IDord-0bbff7524b774ea89cdb78632010a69b
出典メモuspto-grants-1996_07