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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantMethyl 6-formyl-3-methylquinoline-2-carboxylateHCID 19603457—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-Methoxycarbonyl-3-methylquinoline-6-carboxylic acidHCID 1960325880.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994368
Source datasetuspto-grants-1999_11
ORD IDord-b88ee5d0051e45ee9c7bc9e461965360
Source noteuspto-grants-1999_11