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HRID 54013作成日:2026年10月25日

2-Bromobiphenyl → 9-(2-Biphenylyl)-2,7-dibromo-9-fluorenol

https://huagongshe.com/reaction/54013

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromobiphenylHCID 16329—
反応物2,7-Dibromo-9-fluorenoneHCID 259922—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物9-(2-Biphenylyl)-2,7-dibromo-9-fluorenolHCID 22016047—

反応手順

A Grignard reagent prepared from 0.72 g (30 mmol) of magnesium turnings and 5.1 ml (30 mmol) of 2-bromobiphenyl in 15 ml of diethyl ether is added dropwise over the course of 2 hours while stirring (in an ultrasonic bath) to a boiling suspension of 10.0 g (29.6 mmol) of 2,7-dibromo-9-fluorenone in 1 00 ml of dry diethyl ether. After addition is complete, the mixture is boiled for a further 3 hours. After cooling overnight, the precipitate formed is filtered off with suction and washed with cold ether. The magnesium complex filtered off is hydrolyzed in a solution of 15 g of ammonium chloride in 250 ml of ice water. After 1 hour, the 9-(2-biphenylyl)-2,7-dibromo-9-fluorenol formed is filtered off with suction, washed with water and sucked dry. For the ring closure reaction, the dried fluorenol is boiled in 100 ml of glacial acetic acid, after addition of 3 drops of concentrated hydrochloric acid, for 6 hours. The mixture is allowed to crystallize overnight, the product formed is filtered off with suction and washed with glacial acetic acid and water.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621131
出典データセットuspto-grants-1997_04
ORD IDord-3f7abfd6b047478e89dec00d6239ca34
出典メモuspto-grants-1997_04