HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448803Generated: October 29, 2026
Hydrochloric Acid → HCID 59157932, compound
https://huagongshe.com/reaction/448803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloranil | HCID 8371 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Reactant | 4-Bromo-3-iodoaniline | HCID 14548337 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59157932 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08481742B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-ec572221bf684771828d435798781ec8 |
|---|
| Source note | uspto-grants-2013_07 |
|---|