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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-(4-Allyloxybutyloxy)benzoic acid | HCID 21960626 | — |
| Reactant | 9-methyl-9H-fluorene-2,7-diol | HCID 21960627 | — |
| Catalyst | 2-Dimethylaminopyridine | HCID 21885 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,7-Di[4-(4-allyloxybutyloxy)benzoyloxy]-9-methylfluorene | HCID 21960630 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07541071B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-5dc462272ead4de2b68e92f2bb2fb02d |
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| Source note | uspto-grants-2009_06 |
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