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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419818Generated: November 3, 2026

Acetic Acid → HCID 53771658, compound

https://huagongshe.com/reaction/1419818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant1-MethylisoquinolineHCID 15592—
Reactant3-FluorobenzaldehydeHCID 68009—
SolventAcetoneHCID 180—
SolventIsopropanolHCID 3776—
ProductHCID 53771658HCID 5377165878%

Reaction Steps

A mixture of 6.44 g (0.045 mole) of 1-methylisoquinoline, 6.2 g (0.05 mole) of 3-fluorobenzaldehyde and 18 ml of acetic acid is stirred at a temperature between 130° C. and 140° C. for 3 hours. The termination of the reaction is controlled by thin layer chromatography. The reaction mixture is cooled and 100 ml of anhydrous acetone are added to it. Then it is acidified with a mixture of hydrogen chloride and isopropanol until pH=1 under stirring and cooling with ice-water. The suspension is stirred at a temperature between 0° C. and 5° C. for 2 hours. The separated hydrogen chloride salt is filtered, washed with cold acetone and dissolved in 180 ml of water. To the thus-obtained mixture 20% sodium hydroxide solution is dropped until pH=11-12 under stirring and cooling with ice-water, and the solution is extracted three times with 75 ml each of dichloromethane. The extracts are combined, washed with an aqueous sodium chloride solution, dried over Na2SO4 and evaporated. The crude product is recrystallized from 30 ml of isopropanol. Thus 8.7 g (78%) of 1-(3-fluorostyryl)-isoquinoline are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889018
Source datasetuspto-grants-1999_03
ORD IDord-8967093799f840bc90862c6cdd26f62e
Source noteuspto-grants-1999_03