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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978957Generated: October 31, 2026

Benzoyl chloride → HCID 20201043, compound

https://huagongshe.com/reaction/978957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant1,4-Dioxo-3,6-diphenylpyrrolo[3,4-c]pyrroleHCID 15217576—
ProductHCID 20201043HCID 20201043—

Reaction Steps

5.8 Parts of 1,4-diketo-3,6-diphenylpyrrolo-[3,4-c]-pyrrole are stirred with 50 parts of benzoyl chloride at 190° C. for 22 hours. The starting material dissolves in the course of the reaction. On cooling of the reaction mixture, most of the reaction product precipitates. The reaction mixture is introduced into 320 parts of methanol, with stirring, and the mixture is stirred for 2 hours, without heating. The precipitated product is filtered off, washed with methanol and dried. 4.9 parts of ochre-coloured crude product which is purified by crystallisation from 50 parts of dimethylformamide, with addition of a filtration assistant, are obtained. 3.8 parts of 1,4-diketo-2,5-dibenzoyl-3,6-diphenylpyrrolo-[3,4-c]-pyrrole are obtained in the form of brownish-yellow crystals (formula XVIII). ##STR22##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04666455
Source datasetuspto-grants-1987_05
ORD IDord-7b9b182c00dc45c498d95203e5af9e75
Source noteuspto-grants-1987_05