HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889488Generated: October 28, 2026
Hydrochloric Acid → {4-[4,9-Bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetic acid
https://huagongshe.com/reaction/889488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl {4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetate | HCID 58399552 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | {4-[4,9-Bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetic acid | HCID 24739048 | — |
Reaction Steps
Ethyl {4-[4,9-bis(ethyloxy)-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetate (0.050 g, 0.11 mmol) was dissolved in glacial acetic acid (2 ml) and 2N hydrochloric acid (2 ml) added which caused precipitation. The reaction mixture was heated to 100° C. under argon (the precipitate went back into solution) for 2 hours. The reaction mixture was cooled to room temperature and water added with stirring for 5 minutes. A solid precipitate formed which was filtered, washed with water, and collected to give the title compound as a yellow solid. The product was dried overnight in a vacuum oven (0.024 g, 0.05 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252833B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-896a0812e4f3421d9df5a06974942c6a |
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| Source note | uspto-grants-2012_08 |
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