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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253592Generated: November 1, 2026

Oxolinic Acid → 3-Quinolinecarboxylic acid, 1,4-dihydro-6,7-dihydroxy-1-ethyl-4-oxo-

https://huagongshe.com/reaction/2253592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxolinic AcidHCID 4628—
ReactantPotassium HydroxideHCID 14797—
ReactantBoron tribromideHCID 25134—
SolventWaterHCID 962—
Product3-Quinolinecarboxylic acid, 1,4-dihydro-6,7-dihydroxy-1-ethyl-4-oxo-HCID 549301884.1%

Reaction Steps

1.4-Dihydro-1-ethyl-6,7-methylenedioxy-4-oxoquinoline-3-carboxylic acid (3.9 g) and boron tribromide (15 ml) were heated at 50° C. for 15 hours. The reaction mixture was cooled and added slowly to water (100 ml) at 0° C. The pH was adjusted to 11 with concentrated potassium hydroxide, the mixture was filtered and the filtrate taken to pH1, whereupon the precipitate was collected by filtration, washed with water and dried to give 1,4-dihydro-6,7-dihydroxy-1-ethyl-4-oxoquinoline-3-carboxylic acid (3.13 g); δ ((CD3)2SO) 1.42(3H,t); 4.46(2H,q); 7.23(1H,s); 7.66(1H,s); 8.82(1H,s)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232918
Source datasetuspto-grants-1993_08
ORD IDord-0872327a78f3481b8092275f8f211e95
Source noteuspto-grants-1993_08