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HRID 964761作成日:2026年10月27日

9-(2-bromoethyl)-9H-fluorene → 9-(2-Vinylfluorenyl)-2-(9-Fluorenyl)ethane

https://huagongshe.com/reaction/964761

反応式

関与物質

役割名称HCID仕込み量
反応物9-(2-bromoethyl)-9H-fluoreneHCID 11000215—
反応物2-ethenyl-9H-fluoreneHCID 11041607—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物9-(2-Vinylfluorenyl)-2-(9-Fluorenyl)ethaneHCID 86752827—

反応手順

To 1.15 g (6.0 mmol) 2-vinylfluorene in 100 mL diethyl ether was added 3.75 mL (6.0 mmol) n-butyllithium (1.6M in hexane). The reaction mixture was stirred for 4 hours at room temperature. Then 1.64 g (6.0 mmol) 1-bromo-2-(9-fluorenyl)ethane was added and the mixture was stirred for 14 hours at room temperature. The precipitate was removed by filtration, washed with methanol, filtered with pentane using silica gel 60, and concentrated by evaporation under vacuum. The yield was 1.69 g (73%) 1-(9-(2-vinyl)fluorenyl)-2-(9-fluorenyl)ethane as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05770755
出典データセットuspto-grants-1998_06
ORD IDord-cbdacd8506564f279f97bb5941f9fa7c
出典メモuspto-grants-1998_06