HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 2,7-Bis(4-(6-acryloyloxyhexyl)oxybenzoyloxy)fluorene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-((6-(Acryloyloxy)hexyl)oxy)benzoic acid | HCID 3713565 | — |
| Reactant | 9H-Fluorene-2,7-diol | HCID 14938383 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,7-Bis(4-(6-acryloyloxyhexyl)oxybenzoyloxy)fluorene | HCID 22630269 | 22.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06824709B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-e0618c384d974f898d908e9202f951e7 |
| Source note | uspto-grants-2004_11 |