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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982750Generated: November 2, 2026

Water → 2,7-Di[4-(4-allyloxybutyloxy)benzoyloxy]-9-methylfluorene

https://huagongshe.com/reaction/1982750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(4-Allyloxybutyloxy)benzoic acidHCID 21960626—
Reactant9-methyl-9H-fluorene-2,7-diolHCID 21960627—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
Product2,7-Di[4-(4-allyloxybutyloxy)benzoyloxy]-9-methylfluoreneHCID 21960630—

Reaction Conditions

Temperature5 °C

Reaction Steps

1.34 g of 4-(4-allyloxybutyloxy)benzoic acid and 0.46 g of 2,7-dihydroxy-9-methylfluorene were dissolved in 30 ml of methylene chloride and cooled to 5° C. 0.01 g of dimethylaminopyridine and 1.15 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride were added to it, and stirred at room temperature for 12 hours. 50 ml of water was added to it for liquid-liquid separation, and the organic layer was dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the resulting residue was purified through silica gel chromatography, and recrystallized from a mixed solvent of ethanol and ethyl acetate to obtain 0.6 g of 2,7-di[4-(4-allyloxybutyloxy)benzoyloxy]-9-methylfluorene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541071B2
Source datasetuspto-grants-2009_06
ORD IDord-5dc462272ead4de2b68e92f2bb2fb02d
Source noteuspto-grants-2009_06