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HRID 327755作成日:2026年10月26日

Benzene → p-Divinylbenzene

https://huagongshe.com/reaction/327755

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物p-Divinylbenzene benzeneHCID 86746530—
反応物ButyllithiumHCID 178418339—
溶媒HexaneHCID 8058—
生成物p-DivinylbenzeneHCID 66041—

反応手順

Simultaneously, the p-divinylbenzene is distilled from dibutylmagnesium into a clean, flamed and purged valved burette and then diluted by vacuum distillation of 2 times its volume of dry benzene from the stock benzene with n-butyllithium. Next, a clean, flamed and purged, 3-neck, 300 mL reactor flask is fitted with a magnetic stirrer and rubber septum separated from the flask by an in-line, straight-through- bore teflon valve. The burette containing the p-divinylbenzene and benzene is padded with dry argon from the vacuum/argon manifold, the valve is closed and the burette is transferred to the 300 mL reactor flask which is subsequently evacuated and filled with argon several times. Then, about 100 mL benzene is distilled into the reactor flask from the stock benzene/n-butyllithium solution. To the dry benzene in the reactor flask, 0.5 mmoles (0.5 mL of 1.0M solution) of n-butyllithium in hexane is added via gas-tight syringe through the rubber septum and straight-bore valve. After stirring, the reactor flask is cooled to -400° C. and 0.32 mL of the p-divinylbenzene/benzene solution is added dropwise from the burette to give a ratio of p-divinylbenzene to Li+ of 1.5 which produces the micro-particle with the living lithium carbanion initiation sites as indicated by the red-orange color.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05274065
出典データセットuspto-grants-1993_12
ORD IDord-8fe10d2e0d864126b641c347995ae0fe
出典メモuspto-grants-1993_12