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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416362Generated: October 31, 2026

1,2-Dichloroethane → 2,7-Bis(4-(6-acryloyloxyhexyl)oxybenzoyloxy)fluorene

https://huagongshe.com/reaction/2416362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDichloromethaneHCID 6344—
Reactant4-((6-(Acryloyloxy)hexyl)oxy)benzoic acidHCID 3713565—
Reactant9H-Fluorene-2,7-diolHCID 14938383—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product2,7-Bis(4-(6-acryloyloxyhexyl)oxybenzoyloxy)fluoreneHCID 2263026922.3%

Reaction Steps

A mixture of 2,7-dihydroxyfluorene (0.5 g), 4-(6-acryloyloxyhexyloxy)benzoic acid (1.62 g), EDC (1.06 g), DMAP (6.16 mg) and dichloromethane (30 mL) was stirred at a room temperature for 12 hours. Water was added to the reaction mixture to separate an organic layer, and the resulting organic layer was washed with water and dried on anhydrous magnesium sulfate. The solvent was distilled off from this organic layer under reduced pressure, and the resulting residue was purified by means of column chromatography (silica gel, eluting solvent: toluene/ethyl acetate [95/5]) and recrystallization (ethanol/ethyl acetate/toluene) to obtain 2,7-bis(4-(6-acryloyloxyhexyl)oxybenzoyloxy)fluorene (0.42 g) of colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06824709B2
Source datasetuspto-grants-2004_11
ORD IDord-e0618c384d974f898d908e9202f951e7
Source noteuspto-grants-2004_11