HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52608Generated: October 28, 2026
Sodium hydride → N,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole
https://huagongshe.com/reaction/52608
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Reactant | 1,4-Dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole | HCID 15217576 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N'-bis(n-butoxycarbonyl)-1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole | HCID 70191840 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616725 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-66129e337d344ed5a9426bc67e89e139 |
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| Source note | uspto-grants-1997_04 |
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