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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019971Generated: October 30, 2026

Hydrochloric Acid → 3-Methoxy-quinolin-6-ol

https://huagongshe.com/reaction/1019971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantSodium CarbonateHCID 10340—
ReactantSodium NitriteHCID 23668193—
Reactant3-Methoxyquinolin-6-amineHCID 53425796—
SolventWaterHCID 962—
Product3-Methoxy-quinolin-6-olHCID 6674655434%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of sodium nitrite (3.49 g, 50.5 mmol, 1.1 eq) in water (20 mL) is added dropwise at 0° C. to a stirred solution of 3-methoxy-quinolin-6-ylamine (8.0 g, 45.9 mmol, 1.0 eq) in hydrochloric acid (160 mL, 321.3 mmol, 7.0 eq). The mixture is stirred at 0° C. for 2 hours before its addition to a vigorously stirred solution of 10% sulfuric acid (600 mL) at 85-90° C. within 20 minutes. The resulting solution is stirred at 90° C. for 1 hour, cooled down to room temperature, neutralized with sodium carbonate and extracted with ethyl acetate (3×250 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a crude product that is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate:triethylamine, 3:1:0.1, v/v/v) to afford 3-methoxy-quinolin-6-ol as a red solid (2.9 g, 34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716280B2
Source datasetuspto-grants-2014_05
ORD IDord-f1feb0a58c5444f0b27b7108b6423099
Source noteuspto-grants-2014_05