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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448803Generated: October 29, 2026

Hydrochloric Acid → HCID 59157932, compound

https://huagongshe.com/reaction/448803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloranilHCID 8371—
ReactantAmmonium HydroxideHCID 14923—
ReactantCrotonaldehydeHCID 447466—
Reactant4-Bromo-3-iodoanilineHCID 14548337—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductHCID 59157932HCID 59157932—

Reaction Steps

To (4-bromo-3-iodophenyl)amine (11.93 g, 40 mmol) was added cone HCl (6 ml), p-chloranil (9.83 g, 1 equiv.) and isopropanol (20 ml) and the mixture was heated to reflux. A solution of crotonaldehyde (3.98 ml) in isopropanol (3.8 ml) was then added at a rate of 0.1 ml/min using a syringe pump and the mixture was stirred at reflux for another 40 rain after the end of the addition. The mixture was cooled to r.t., dilated with EtOAc and 5% aq. NH4OH. The products were extracted in EtOAc and the organic layer was washed several times with water, brine, and dried over Na2SO4. The crude material was dissolved as much as possible in 300 ml boiling toluene and purified by flash chromatography on silica with a gradient of EtOAc/toluene 0 to 5%. The first product was 6-bromo-7-iodo-2-methylquinoline followed by its isomer 6-bromo-5-iodo-2-methylquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481742B2
Source datasetuspto-grants-2013_07
ORD IDord-ec572221bf684771828d435798781ec8
Source noteuspto-grants-2013_07