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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375402Generated: October 28, 2026

Sodium hydride → N,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole

https://huagongshe.com/reaction/375402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantButyl chloroformateHCID 61140—
Reactant1,4-Dioxo-3,6-diphenylpyrrolo[3,4-c]pyrroleHCID 15217576—
SolventTetrahydrofuranHCID 8028—
ProductN,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrroleHCID 7019184073%

Reaction Steps

To a suspension of 0.5 g (0.00175 mol) of 1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole in 17 ml of tetrahydrofuran are added, under argon, 0.28 g (0.007 mol) of solid sodium hydride. After stirring for 24 hours, 0.67 ml (0.007 mol) of n-butyl chloroformate are added and the suspension is stirred overnight. The mixture is filtered and the filtrate is concentrated under vacuum. The residue is taken up in water/diethyl ether, the organic phase is dried over MgSO4 and then concentrated under vacuum. The residue is taken up in n-hexane and the precipitated yellow powder is collected by filtration and washed with a minor amount of n-hexane, giving 0.62 g (73% of theory) of N,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole as a yellow fluorescent powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484943
Source datasetuspto-grants-1996_01
ORD IDord-cfd695cb536e44cb8decdccbcefa7a58
Source noteuspto-grants-1996_01