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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630646Generated: October 30, 2026

Water → HCID 86237345, compound

https://huagongshe.com/reaction/630646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium IodideHCID 4875—
ReactantPotassium HydroxideHCID 14797—
Reactant2-AcetylfluoreneHCID 69908—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86237345HCID 86237345181.3%

Reaction Conditions

Temperature15 °C

Reaction Steps

15.9 g of 2-acetylfluorene (11) (76.4 mmol), 18.9 g of potassium hydroxide (0.27 mol, purity: 80%), and 1.26 g of potassium iodide (7.6 mmol) were dissolved in 350 ml of anhydrous dimethylsulfoxide under nitrogen atmosphere, and a reaction temperature was maintained at 15° C. Then, 33 ml of n-bromobutane (0.3 mol) was slowly added thereto for 2 hours, followed by stirring at 15° C. for 1 hour. Thereafter 200 ml of distilled water was added to the reaction mixture and stirred for about 30 minutes, a product was extracted with 300 ml of dichloromethane, and the extracted organic layer was washed with 100 ml of distilled water three times. Then, the recovered organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled under reduced pressure. The obtained product was purified using a silica gel column chromatography (developing solvent: dichloromethane:n-hexane=15:1), thereby obtaining 22.2 g of 1-(9,9-di-n-butylfluorene-2-yl)-ethanone (12) (90.8%) as a light yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09316906B2
Source datasetuspto-grants-2016_04
ORD IDord-56f62b04df0c474884c03f8fe2fdf2bd
Source noteuspto-grants-2016_04