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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649422Generated: October 31, 2026

Phosphoric Acid → 8-(p-toluenesulfonyloxy)-6,7-dihydro-1-oxo-1H,5H-benzo-[ij]quinolizine-2-carboxylic acid

https://huagongshe.com/reaction/1649422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant5-(p-Toluenesulfonyloxy)-1,2,3,4-tetrahydroquinolineHCID 12899679—
Reactant3-Ethoxy-2-ethoxycarbonylprop-2-enoateHCID 85829211—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product8-(p-toluenesulfonyloxy)-6,7-dihydro-1-oxo-1H,5H-benzo-[ij]quinolizine-2-carboxylic acidHCID 1289968169.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

21.6 g of ethyl ethoxymethylenemalonate was added to 30.0 g of 5-(p-toluenesulfonyloxy)-1,2,3,4-tetrahydroquinoline and the mixture was heated at 110° C. on an oil bath for 30 minutes while stirring, during which time distillation of ethanol was observed. After heating, 240 g of polyphosphoric acid prepared from 120 g of phosphoric acid and 120 g of phosphorus pentoxide was added to the mixture and the mixture was allowed to react on an oil bath at 140° C. for 40 minutes. After completion of the reaction, the mixture was allowed to cool to room temperature and poured into 400 ml of water, followed by rendering the mixture neutral with a 40% aqueous sodium hydroxide to precipitate crystals. The crystals thus-obtained were mixed with 150 ml of a 10% aqueous sodium hydroxide solution and the mixture was heat refluxed for 40 minutes during which time the crystals were dissolved to form a uniform solution. The solution was filtered and the filtrate was allowed to cool and adjusted to a pH of 2 to precipitate crystals which were collected by filtration. Recrystallization of the crude crystals thus-obtained from dimethylformamide gave 27.4 g of an 8-(p-toluenesulfonyloxy)-6,7-dihydro-1-oxo-1H,5H-benzo-[ij]quinolizine-2-carboxylic acid as white needles having a melting point of not lower than 300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04416884
Source datasetuspto-grants-1983_11
ORD IDord-4a7575aa6d6c4c568f654e71567566dd
Source noteuspto-grants-1983_11