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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981194Generated: October 30, 2026

Chloroform → 2-Chloro-6,7-difluoro-3-formyl-1,4-dihydroquinoline

https://huagongshe.com/reaction/981194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
Reactant6,7-Difluoro-3,4-dihydroquinolin-2(1h)-oneHCID 14853334—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Chloro-6,7-difluoro-3-formyl-1,4-dihydroquinolineHCID 14853335—

Reaction Steps

76.9 cm3 of phosphoryl chloride are added in the course of 30 minutes, with stirring, at between 10° and 15° C., to a mixture of 800 cm3Of trichloromethane and 74.35 cm3 of dimethylformamide and the mixture is stirred for 1 hour at a temperature close to 20° C. 65.8 g of 6,7-difluoro-3,4-dihydrocarbostyril are added in the course of 10 minutes, at about 20° C., with vigorous stirring, to the solution obtained The solution obtained is heated to a temperature close to 60° C. and kept at this temperature for 2 hours. The reaction mixture is concentrated under reduced pressure (20 kPa) at 50° C. until a pasty mixture is obtained. A mixture of 500 g of ice and 500 cm3 of water is added, with vigorous stirring. The solid obtained is drained at about 5° C. and washed with 3 times 300 cm3 of water at 5° C. The moist product obtained and 60 g of sodium acetate are added simultaneously, in the course of 1 hour, to 1.5 liters of water at 90° C., in such a way as to maintain the pH at about 6. The mixture is stirred for a further 30 minutes at 90° C., the temperature is allowed to fall to about 50° C. and the product is drained at this temperature and washed with 3 times 300 cm3 of water at about 20° C. 70.18 g of 2-chloro-6,7-difluoro-3-formyl-1,4-dihydroquinoline are obtained in the form of a yellow solid melting at 260° C., which is used in this form for the subsequent steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990515
Source datasetuspto-grants-1991_02
ORD IDord-16061b0244b94280aab9ee1d73632530
Source noteuspto-grants-1991_02