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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523128Generated: October 31, 2026

Hydrochloric Acid → HCID 59157932, compound

https://huagongshe.com/reaction/523128

Reaction equation

Participants

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

Reaction Steps

To (4-bromo-3-iodophenyl)amine (11.93 g, 40 mmol) was added conc 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 min after the end of the addition. The mixture was cooled to r.t., diluted 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 numberUS09334295B2
Source datasetuspto-grants-2016_05
ORD IDord-2f901d0511f64b24b0f9cbdccb4b102f
Source noteuspto-grants-2016_05