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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049555Generated: November 1, 2026

Oxalyl chloride → Pyrrolo[3,2,1-ij]quinoline-1,2-dione

https://huagongshe.com/reaction/2049555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1,2-DihydroquinolineHCID 5231402—
ProductPyrrolo[3,2,1-ij]quinoline-1,2-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198414
Source datasetuspto-grants-1980_04
ORD IDord-644488113e584a4990e5d7683bc7e3ab
Source noteuspto-grants-1980_04