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HRID 15688作成日:2026年10月27日

Phloroglucinol → 1,3,5-Tris(vinyloxy)benzene

https://huagongshe.com/reaction/15688

反応式

関与物質

役割名称HCID仕込み量
反応物PhloroglucinolHCID 359—
反応物Vinyl AcetateHCID 7904—
反応物Sodium CarbonateHCID 10340—
反応物1-Hydroxy-3,5-bis(vinyloxy)benzeneHCID 22935762—
反応物1,3-Dihydroxy-5-vinyloxybenzeneHCID 22935814—
溶媒TolueneHCID 1140—
生成物1,3,5-Tris(vinyloxy)benzeneHCID 11820226—

反応条件

温度100 °C

反応手順

To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (67 mg, 0.1 mmol) and sodium carbonate (640 mg, 6 mmol) in toluene (5 ml) were added 1,3,5-trihydroxybenzene (5 mmol) and vinyl acetate (2.15 g, 25 mmol), followed by stirring at 100° C. in an atmosphere of argon gas for 6 hours. The reaction mixture was analyzed by gas chromatography to find that 1,3-dihydroxy-5-vinyloxybenzene, 1-hydroxy-3,5-bis(vinyloxy)benzene, and 1,3,5-tris(vinyloxy)benzene were formed in yields of 5%, 4%, and 18%, respectively, with a conversion from 1,3,5-trihydroxybenzene of 29%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732645B2
出典データセットuspto-grants-2010_06
ORD IDord-8ef2f81780604f299e5c56be6d35d965
出典メモuspto-grants-2010_06