HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrobenzene → HCID 20028938, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 4-Amino-2-methylquinoline | HCID 81116 | — |
| Product | HCID 20028938 | HCID 20028938 | — |
Reaction Steps
The starting material was prepared as follows. A solution of 4-amino-2-methylquinoline (5.0 g.) and allyl bromide (3.32 ml.) in nitrobenzene (13.7 ml.) was stirred at 100° for 1 hour. The reaction mixture was cooled to below 5° and the resulting precipitate filtered off, washed with ether and dried. A suspension of this material in N aqueous NaOH (75 ml.) was stirred at 100° for 3.5 hours. The cooled mixture was extracted with EtOAc (2×75 ml.) and the combined extracts washed, dried and evaporated to give 1-allyl-2-methyl-4-quinolone. Reaction of this compound with toluene-p-sulphonyl chloride gave 1-allyl-4-chloro-2-methylquinolinium toluene-p-sulphonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855420 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-a2a8f8c8a2ed4af7a3f133515ce6fbfa |
| Source note | uspto-grants-1989_08 |