HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Isobenzofurandione, 5-fluoro- → 9,9-Bis{4-(4-fluorophthalimido)phenyl}fluorene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Isobenzofurandione, 5-fluoro- | HCID 67572 | — |
| Reactant | 4,4'-(9-Fluorenylidene)dianiline | HCID 631552 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 9,9-Bis{4-(4-fluorophthalimido)phenyl}fluorene | HCID 15300702 | — |
Reaction Steps
A mixture of 9,9-bis(4-aminophenyl )fluorene (17.4 g, 50 mmol), 4-fluorophthalic anhydride (18.3 g, 110 mmol), and 250 ml of acetic acid was stirred and heated under reflux for five hours and then stirred at ambient temperature overnight. A colorless precipitate formed which was filtered, washed twice with 150 ml of ethanol, washed twice with 100 ml of hexane, suction-dried for two hours, and then dried in a vacuum oven at 120° C. for 16 hours. The title compound was isolated as a colorless powder (29.2 g, 90.6% yield) that had melting point of 323.5°-326° C. and a 1H NMR spectrum (DMSO-d6) corresponding to δ8.02 (m, 4H), 7.86 (dd, 2H), 7.72 (m, 2H), 7.60 (d, 2H), 7.46 (t, 2H), and 7.35 (m, 10H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05386002 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-a449b3f95269440b93c44d24a1295dc5 |
| Source note | uspto-grants-1995_01 |