HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476811Generated: October 31, 2026
Potassium Hydroxide → 8-Fluoro-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid
https://huagongshe.com/reaction/1476811
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (Z)-methyl 2-fluoro-6-((5-oxo-2-phenyloxazol-4(5H)-ylidene)methyl)benzoate | HCID 90387079 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 8-Fluoro-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid | HCID 90387187 | 41.9% |
Reaction Steps
A solution of crude (Z)-methyl 2-fluoro-6-((5-oxo-2-phenyloxazol-4(5H)-ylidene)methyl)benzoate (15 g) and potassium hydroxide (2.58 g, 46 mmol) in acetic anhydride (150 mL) was heated at 100° C. for 2 hours. The solvent was removed in vacuo, and the residue was diluted with water (30 mL). The resulting mixture was neutralized with 1M aqueous HCl (100 mL) and filtered. The solids were dried in vacuo to give 8-fluoro-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid (4 g, ESI-MS m/z [M+H]+ 208.0) which was converted to the methyl ester as described, below. The filtrate was concentrated under reduced pressure to give crude product which was purified by column chromatography eluting with a gradient of EtOAc (30-100%) and PE to give a first batch of the title compound (2 g, 19.6%). ESI-MS m/z [M+H]+=222.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09402841B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e6a5362e53c34fdca6ec09ab17b4b5e3 |
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| Source note | uspto-grants-2016_08 |
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