HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609507Generated: October 25, 2026
Water → 1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehyde
https://huagongshe.com/reaction/1609507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Hydroxyquinoline-3-carbaldehyde | HCID 589334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehyde | HCID 4914628 | 74% |
Reaction Steps
Sodium hydride (55% w/w suspension in oil; 0.268 g) was added portionwise to a stirred suspension of 1,2-dihydro-2-oxoquinoline-3-carbaldehyde (1 g) in dimethylformamide (10 ml) which had been cooled in an ice bath. The mixture was allowed to warm to ambient temperature and was then heated to 60° C. for 1 hour. The mixture was recooled in an ice bath and methyl iodide (0.41 ml) was added. Dimethylformamide (50 ml) was added and the mixture was stirred at ambient temperature for 16 hours. The mixture was poured into water (50 ml) and extracted with methylene chloride (3×50 ml). The combined extracts were washed with water (50 ml) and evaporated. The residue was triturated under diethyl ether to give 1,2-dihydro-1-methyl-2-oxoquinoline-3-carbaldehyde as a pale yellow solid (0.81 g, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401751 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-8163d9ba4b404caaaa340f83b033a8bf |
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| Source note | uspto-grants-1995_03 |
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