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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754559Generated: October 28, 2026

Hydrochloric Acid → 7-bromo-4-hydroxy-1-(propan-2-yl)quinolin-2(1H)-one

https://huagongshe.com/reaction/1754559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 7-bromo-2,4-dioxo-1-(propan-2-yl)-1,2,3,4-tetrahydroquinoline-3-carboxylateHCID 86679803—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-bromo-4-hydroxy-1-(propan-2-yl)quinolin-2(1H)-oneHCID 8667980491%

Reaction Steps

A suspension of ethyl 7-bromo-2,4-dioxo-1-(propan-2-yl)-1,2,3,4-tetrahydroquinoline-3-carboxylate (1.5 g, 4.23 mmol) in sodium hydroxide (2M solution, 32 mL, 64 mmol) is heated to reflux. The reaction medium becomes homogeneous and, after 3 hours, a suspension is once again observed. 6 mL of NMP are added to homogenize, and the resulting mixture is than refluxed for 12 hours. The solution cooled to room temperature is poured into 6M hydrochloric acid solution to give a white precipitate, which is filtered off. After rinsing with water and drying the precipitate under vacuum, 1.1 g of a white solid are obtained (yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169246B2
Source datasetuspto-grants-2015_10
ORD IDord-04190063de69446aba03eb70a7df73d6
Source noteuspto-grants-2015_10