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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725153Generated: October 26, 2026

Diethyl Ether → 9-(2-Biphenylyl)-2-bromo-9-fluorenol

https://huagongshe.com/reaction/1725153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2-BromobiphenylHCID 16329—
ReactantMagnesiumHCID 5462224—
Reactant2-BromofluorenoneHCID 66810654—
Catalyst1,1-DibromoethaneHCID 11201—
Product9-(2-Biphenylyl)-2-bromo-9-fluorenolHCID 2256437390%

Reaction Steps

A 100 ml three neck distilling flask was charged with magnesium (1.26 g, 0.052 mol). Vacuum was formed in a system. The magnesium was heated to stir for 30 minutes to be activated. After cooling to room temperature, nitrogen gas stream was formed in the system. Then, 5 ml diethyl ether and a few drops of dibromoethane were added. And then, 2-bromobiphenyl (11.65 g, 0.050 mol) dissolved in 15 ml diethyl ether was slowly dropped. After dropping, the reaction was refluxed for 3 hours to be a Grignard reagent. A 200 ml three neck distilling flask was charged with 2-bromofluorenone (11.7 g, 0.045 mol) and 40 ml diethyl ether. The synthesized Grignard reagent was slowly dropped to the reacted solution. After the dropping, the solution was refluxed for 2 hours and stirred at room temperature overnight. After reaction, the reacted solution was washed with saturated ammonium chloride solution twice, and a water layer was extracted with ethyl acetate twice and washed with saturated salt solution twice with an organic layer. After drying with magnesium sulfite, the reacted solution was suctioned and filtrated, and condensed to give 18.76 g 9-(2-biphenylyl)-2-bromo-9-fluorenol in a solid state in a yield of 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488849B2
Source datasetuspto-grants-2009_02
ORD IDord-2d509e6bb104460a9d76c4c51262162f
Source noteuspto-grants-2009_02