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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413962Generated: October 25, 2026

8,9-dichloro-5-methyl-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid ethyl ester → 8,9-dichloro-5-methyl-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid

https://huagongshe.com/reaction/2413962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8,9-dichloro-5-methyl-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid ethyl esterHCID 13960201—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
Product8,9-dichloro-5-methyl-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acidHCID 2015434686%

Reaction Steps

7.08 g (0.02 mole) of 8,9-dichloro-5-methyl-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid ethyl ester was suspended in a mixture of 14 ml of concentrated hydrochloric acid and 56 ml of acetic acid, and this suspension was stirred at 110°-120° C. for 3 hours to hydrolyze the starting material. The resulting reaction solution was allowed to cool to room temperature. The precipitate which separated out was collected by filtration and washed with water to obtain 5.61 g (86.0% yield) of 8,9-dichloro-5-methyl-6,7-dihydro-1,7-dioxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid in the form of pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04720495
Source datasetuspto-grants-1988_01
ORD IDord-18a7c564e47c42f7999a0a2ffd0b66a9
Source noteuspto-grants-1988_01