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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54013생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/54013

반응식

참여 물질

역할이름HCID투입량
반응물2-BromobiphenylHCID 16329—
반응물2,7-Dibromo-9-fluorenoneHCID 259922—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
생성물9-(2-Biphenylyl)-2,7-dibromo-9-fluorenolHCID 22016047—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05621131
출처 데이터셋uspto-grants-1997_04
ORD IDord-3f7abfd6b047478e89dec00d6239ca34
출처 메모uspto-grants-1997_04