HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604550Generated: October 30, 2026
Hydrochloric Acid → 2-Methoxycarbonyl-3-methylquinoline-6-carboxylic acid
https://huagongshe.com/reaction/1604550
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Methyl 6-formyl-3-methylquinoline-2-carboxylate | HCID 19603457 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-Methoxycarbonyl-3-methylquinoline-6-carboxylic acid | HCID 19603258 | 80.8% |
Reaction Steps
To a mixture of water (0.8 ml) and tert-butyl alcohol (3 ml) were added methyl 6-formyl-3-methylquinoline-2-carboxylate (140 mg) , 2-methyl-2-butene (190 mg) and sodium dihydrogenphosphate (105 mg) in water bath. To the mixture was added dropwise sodium chloride (244 mg) and the mixture was stirred for 1 hour at the same temperature. The reaction mixture was cooled in an ice bath, adjusted to pH 4 with 1M hydrochloric acid and extracted with dichloromethane. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (dichloromethane:methanol=10:1, V/V) followed by crystallization from methanol-isopropyl ether to give 2-methoxycarbonyl-3-methylquinoline-6-carboxylic acid (121 mg) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994368 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-b88ee5d0051e45ee9c7bc9e461965360 |
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| Source note | uspto-grants-1999_11 |
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