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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981185Generated: October 30, 2026

Chloroform → 2,7-Dichloro-6-fluoro-3-formyl-1,4-dihydroquinoline

https://huagongshe.com/reaction/981185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
Reactant7-Chloro-6-fluoro-3,4-dihydrocarbostyrilHCID 14700544—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2,7-Dichloro-6-fluoro-3-formyl-1,4-dihydroquinolineHCID 14700545—

Reaction Steps

55.6 cm3 of phosphoryl chloride are added in the course of 30 minutes, with stirring, at between 10° and 15° C., to a mixture of 250 cm3 of trichloromethane and 54 cm3 of dimethylformamide and the mixture is stirred for 1 hour at a temperature close to 20° C. 52 g of 7-chloro-6-fluoro-3,4-dihydrocarbostyril are added progressively, with vigorous stirring, in the course of 10 minutes, at about 20° C. to the solution obtained. The suspension obtained is heated to a temperature close to 60° C. and is kept at this temperature for a further 2 hours, with stirring. The reaction mixture is concentrated under reduced pressure (20 kPa) at 50° C. until a pasty mixture is obtained. A mixture of 250 cm3 of water and 250 g of crushed ice is added, with vigorous stirring. The solid obtained is drained at about 5° C. and washed with 4 times 125 cm3 of water at 5° C. The moist product obtained and 58 g of sodium acetate are added simultaneously, in the course of 1 hour, to 500 cm3 of water at 90° C. in such a way as to maintain the pH at about 6. The mixture is stirred for a further 15 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 250 cm3 of water at about 20° C. 54.3 g of 2,7-dichloro-6-fluoro-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-13350241b37643acaea18033843e0d8d
Source noteuspto-grants-1991_02