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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160980Generated: October 31, 2026

2-Bromobiphenyl → 9-(2-Biphenylyl)-2-bromo-9-fluorenol

https://huagongshe.com/reaction/1160980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobiphenylHCID 16329—
Reactant2-Bromo-9-fluorenoneHCID 725831—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product9-(2-Biphenylyl)-2-bromo-9-fluorenolHCID 2256437390%

Reaction Steps

1.26 g (0.052 mol) of magnesium was put in a 100 mL three-necked flask to which a dropping funnel and a Dimroth condenser were connected, and the flask was evacuated. The magnesium was activated by 30 minutes of heating and stirring. After cooling to room temperature, the flask was placed under a nitrogen gas flow. 5 mL of diethyl ether and several drops of dibromoethane were added, and 11.65 g (0.050 mol) of 2-bromobiphenyl dissolved in 15 mL of diethyl ether was slowly delivered from the dropping funnel by drops into the mixture. After the dropping was complete, the mixture was refluxed for 3 hours and made into a Grignard reagent. 11.7 g (0.045 mol) of 2-bromo-9-fluorenone and 40 mL of diethyl ether were put in a 200 mL three-necked flask to which a dropping funnel and a Dimroth condenser were connected. To this reaction solution, the synthesized Grignard reagent was slowly delivered by drops from the dropping funnel. After the dropping was complete, the mixture was refluxed for 2 hours, and then stirred at room temperature for about 12 hours. After the reaction was complete, the solution was washed twice with saturated ammonia chloride solution. An aqueous layer was extracted twice with ethyl acetate and combined with an organic layer, and the solution was washed with a saturated saline solution. After drying with magnesium sulfate, suction filtration and concentration were conducted, and a solid of 9-(biphenyl-2-yl)-2-bromo-9-fluorenol was obtained, weighing 18.76 g in a yield of 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816668B2
Source datasetuspto-grants-2010_10
ORD IDord-69e9dc58edd64b14b0252f45c2ed962d
Source noteuspto-grants-2010_10