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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020011Generated: November 2, 2026

Methanol → Methyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylate

https://huagongshe.com/reaction/1020011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Carboxymethylbenzaldehyde hippuric acidHCID 86664383—
ProductMethyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylateHCID 64118399%

Reaction Conditions

Temperature65 °C

Reaction Steps

The 2-carboxymethylbenzaldehyde hippuric acid adduct from above (1.0 g, 3.3 mmoles) was dissolved in methanol (20 mls) and solid potassium hydroxide (0.37 g, 6.6 mmoles) was added. The clear solution was heated (65° C.) for 1 hour. The reaction was evaporated and the solid residue partitioned between water (25 mls) and ethyl acetate (25 mls). The aqueous layer was further extracted with ethyl acetate (2×10 mls) and the combined ethyl acetate extracts washed with brine (10 mls) water (10 mls). After drying over magnesium sulphate the solution was evaporated to leave a yellow solid (0.68 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716302B2
Source datasetuspto-grants-2014_05
ORD IDord-56c1c7c8a4854d16bb6e3ee30938b9b2
Source noteuspto-grants-2014_05