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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant(Z)-methyl 2-fluoro-6-((5-oxo-2-phenyloxazol-4(5H)-ylidene)methyl)benzoateHCID 90387079—
SolventAcetic AnhydrideHCID 7918—
Product8-Fluoro-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acidHCID 9038718741.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402841B2
Source datasetuspto-grants-2016_08
ORD IDord-e6a5362e53c34fdca6ec09ab17b4b5e3
Source noteuspto-grants-2016_08