Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448826Generated: October 31, 2026

Carbon Dioxide → HCID 12802778, compound

https://huagongshe.com/reaction/1448826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant1-[(3,4-Dichlorophenyl)methyl]-7-fluoro-4-methylquinolin-2(1H)-oneHCID 20375612—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventTriethylamineHCID 8471—
ProductHCID 12802778HCID 1280277866%

Reaction Steps

1-(3,4-Dichlorobenzyl)-1,2-dihydro-7-fluoro-4-methyl-2-oxoquinoline (7 g.) was added portionwise to a solution of n-butyl-lithium (9.8 ml. of a 2.32 N-solution in hexane) and triethylamine (1.15 g.) in dry tetrahydrofuran (150 ml.) maintained at -40° C. The mixture was stirred at -30° C. to -40° C. for one hour under an atmosphere of dry argon, and then added to a saturated solution of dry carbon dioxide in dry tetrahydrofuran (200 ml.). The mixture was stirred at -30° C. for 2 hours and then allowed to reach ambient temperature overnight. Water (400 ml.) was added and the concentrated hydrochloric acid to bring the pH of the mixture to 3-4. The crude acid was filtered off and recrystallised from methanol to give 1-(3,4-dichlorobenzyl)-1,2-dihydro-7-fluoro-2-oxoquinol-4-ylacetic acid, m.p. 205°-207° C. (dec.), in 66% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04187310
Source datasetuspto-grants-1980_02
ORD IDord-577cd0ef7c014c38923efcd4b3272cb1
Source noteuspto-grants-1980_02