HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636070Generated: October 30, 2026
Aluminum(III) Chloride → HCID 11457997, compound
https://huagongshe.com/reaction/636070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | HCID 131722398 | HCID 131722398 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 11457997 | HCID 11457997 | 92% |
Reaction Steps
A solution of compound 2 (19.0 g, 67.1 mmol) in chlorobenzene (120 mL) was taken in a 500 mL round bottom flask equipped with a mechanical stirrer and a reflux condenser. Aluminium chloride (44.6 g, 335.6 mmol) was added in portions over a period of 10 min. The reaction mixture was heated at 130° C. for 3 h and cooled to room temperature (TLC chloroform: methanol 9:1, Rf=0.2). Poured into crushed ice (1 Kg) and stirred at room temperature for further 30 min. The solid separated was filtered and washed with water till neutral to pH. The solid was then washed with hexane (2×50 mL) and dried at 100° C. for 1 h to furnish 5,7-dihydroxy-1,2-dihydro-2-quinolinone (3, 10 g) in 92% yield as a dark brown solid. M.P.>300° C. The quinolinone obtained was further characterised as its diacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06191279B1 |
|---|
| Source dataset | uspto-grants-2001_02 |
|---|
| ORD ID | ord-a3902062c6e3465bb9c4ed6bc9326b13 |
|---|
| Source note | uspto-grants-2001_02 |
|---|