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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744751Generated: October 29, 2026

Ethanol → 2-Butoxy-1,8-difluoro-7-(4-n-pentylphenyl)fluorene

https://huagongshe.com/reaction/1744751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-4-pentylbenzeneHCID 2735599—
Reactant7-Butoxy-1,8-difluorofluorene-2-boronic acidHCID 22223115—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-Butoxy-1,8-difluoro-7-(4-n-pentylphenyl)fluoreneHCID 22223123—

Reaction Steps

12 mmol of 7-butoxy-1,8-difluorofluorene-2-boronic acid (Example 6, 1st stage), 20 ml of ethanol, a solution of 24 mmol of sodium carbonate in 20 ml of water and 1 mol % of tetrakis(triphenylphosphine)palladium(0) are added to a solution of 12 mmol of 4-n-pentylbromobenzene in 40 ml of toluene. The mixture is heated to boiling until the reaction is complete. After cooling, the mixture is admixed with 100 ml of water, the phases are separated and the aqueous phase is extracted with toluene. The combined organic phases are washed with saturated NaCI solution and dried over sodium sulfate, and the solvents are removed under reduced pressure. The crude product is chromatographed on silica gel (2:5 dichloromethane/heptane) and recrystallized from heptane. 2-Butoxy-1,8-difluoro-7-(4-n-pentylphenyl)fluorene is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07018685B2
Source datasetuspto-grants-2006_03
ORD IDord-542bfa57cec64f758f5d247622e8e011
Source noteuspto-grants-2006_03