Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844289Generated: November 1, 2026

Dimethylformamide → HCID 66822907, compound

https://huagongshe.com/reaction/1844289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant3,6-Bis(5-bromothiophen-2-yl)-2,5-dihexyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dioneHCID 66822894—
ReactantHCID 178418546HCID 178418546—
ProductHCID 66822907HCID 66822907—

Reaction Conditions

Temperature130 °C

Reaction Steps

The synthesis of 2,5-di-n-hexyl-3,6-bis(5-bromo-thiophen-2-yl)pyrrolo[3,4-c]-pyrrole-1,4-dione is done in analogy to Zhou et al., Macromolecules 43 (2010) 821-826. 2,5-Di-n-hexyl-3,6-bis(5-bromo-thiophen-2-yl)pyrrolo[3,4-c]-pyrrole-1,4-dione (237 mg, 0.378 mmol) and copper(I)-cyanide (1.50 g, 17.0 mmol) are placed in a 25 mL-flask under argon. Dry DMF (10 mL) is added and the mixture is stirred at 130° C. for 4 h. The solvent is removed under reduced pressure and the residual solid is extracted with chloroform (250 mL). After removing the solvent the crude product is purified by column chromatography (dichloromethane). A violet solid is obtained (52 mg, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946376B2
Source datasetuspto-grants-2015_02
ORD IDord-12533007a2494a5b9739efc60514a263
Source noteuspto-grants-2015_02