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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Carboxymethylbenzaldehyde hippuric acid | HCID 86664383 | — |
| Product | Methyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylate | HCID 641183 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716302B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-56c1c7c8a4854d16bb6e3ee30938b9b2 |
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| Source note | uspto-grants-2014_05 |
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