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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410321Generated: October 30, 2026

Fluorene → HCID 22568527, compound

https://huagongshe.com/reaction/1410321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluoreneHCID 6853—
ReactantMyristyl bromideHCID 8208—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22568527HCID 22568527166.5%

Reaction Conditions

Temperature10 °C

Reaction Steps

A 2000 mL round flask was charged with 9H-fluorene (15 g, 90.24 mmol) and potassium tert-butoxide (21.2 g, 198.5 mmol), and then 300 mL of DMSO was slowly injected thereto. Under nitrogen atmosphere, 1-bromotetradecane (54 g, 198.5 mmol) was slowly dropped through a dropping funnel while the reactor temperature was maintained at 10° C. or lower. The mixture was stirred at room temperature for 24 hours, and the reaction was terminated by addition of 500 mL of distilled water. The organic layer collected by extraction with n-hexane was dried over magnesium sulfate, followed by removal of volatile materials, and then purified with n-hexane by using silica gel column chromatography tube, followed by drying, to thereby obtain 42.0 g of 9,9-ditetradecyl-9H-fluorene (yield: 83.26%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921499B2
Source datasetuspto-grants-2014_12
ORD IDord-45649e8ff39f44269617a655908616a8
Source noteuspto-grants-2014_12