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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253074Generated: October 25, 2026

Hydrochloric Acid → 4-Methylquinoline-6-carbonitrile hydrochloride

https://huagongshe.com/reaction/253074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl vinyl ketoneHCID 6570—
ReactantChloranilHCID 8371—
Reactant4-AminobenzonitrileHCID 13396—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4-Methylquinoline-6-carbonitrile hydrochlorideHCID 6686655182.55%

Reaction Conditions

Temperature75 °C

Reaction Steps

Add 95% ethanol (EtOH) (270 L, 9 vol.), 4-aminobenzonitrile (30.0 kg, 1 equiv) and 2,3,5,6-tetrachloro-2,5-cyclohexadiene-1,4-dione, (66.81 kg 1.07 equiv) to a 200 gallon reaction vessel equipped with nitrogen purge, condenser, thermocouple, and overhead agitation. Stir for 2-5 min, then add concentrated hydrochloric acid (HCl) (62.56 L, 3.0 equiv), then heat to 75° C. Dilute methyl vinylketone (33.06 L, 1.5 equiv) in 95% EtOH (30 L, 1 vol.) then add slowly to reaction mixture over 30 min. Monitor for reaction completion by high performance liquid chromatography (HPLC). Add tetrahydrofuran (THF) (11 vol., 330 L), at 75° C., then stir for 1 hour at 60° C. Cool to room temperature and stir for 1 additional hour. Filter on agitated filter/dryer, then rinse with THF (240 L, 8 volumes). Dry overnight under vacuum at 70° C. to give the title compound (42.9 kg, 82.55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872020B2
Source datasetuspto-grants-2011_01
ORD IDord-be82749e844544239a8c401e06537fe7
Source noteuspto-grants-2011_01