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HRID 1633820생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1633820

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 was added dropwise to a boiling suspension of 10.0 g (29.6 mmol) of 2,7-dibromo-9-fluorenone in 100 ml of dry diethyl ether in the course of 2 hours, while stirring (in an ultrasonic bath). When the addition had ended, the mixture was boiled for a further 3 hours. After cooling overnight, the precipitate which had separated out was filtered off with suction and washed with cold ether. The magnesium complex which had been filtered off with suction was 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 was filtered off with suction, washed with water and sucked dry. For the cyclization reaction, the dried fluorenol was boiled in 100 ml of glacial acetic acid, after addition of 3 drops of concentrated hydrochloric acid, for 6 hours. The mixture was left to crystallize overnight and the product formed was filtered off with suction and washed with glacial acetic acid and water.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06504042B1
출처 데이터셋uspto-grants-2003_01
ORD IDord-e0a6321661c3499f84b87c054f138b5b
출처 메모uspto-grants-2003_01