HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → Pyrrolo[3,2,1-ij]quinoline-1,2-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1,2-Dihydroquinoline | HCID 5231402 | — |
| Product | Pyrrolo[3,2,1-ij]quinoline-1,2-dione | HCID 66552534 | — |
Reaction Steps
Generally speaking, the reaction of a 1,2-dihydroquinoline (II) with oxalyl chloride (III) to give a 4-H-pyrrolo[3,2,1-ij]quinolin-1,2-dione (I) is carried out in a dry aprotic solvent by the dropwise addition of a solution of the 1,2-dihydroquinoline in the same solvent to the stirred solution of oxalyl chloride in an inert atmosphere at or near room temperature. Subsequent to the addition the reaction mixture is briefly stirred at ambient temperature and then at gentle reflux to complete the reaction. The solvent is stripped from the reaction mixture at reduced pressure to give a solid residue which on crystallization from a selected solvent or solvent system furnishes the 4-pyrrolo[3,2,1-ij]quinoline-1,2-dione I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198414 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-644488113e584a4990e5d7683bc7e3ab |
| Source note | uspto-grants-1980_04 |