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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892383Generated: October 25, 2026

Dicyclohexylcarbodiimide → 2,3-Dicyano-4-hexyloxyphenyl 5-hexylthiophene-2-carboxylate

https://huagongshe.com/reaction/892383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(Pyrrolidin-1-yl)pyridineHCID 11019020—
Reactant5-Hexyl-2-thiophenecarboxylic acidHCID 13128269—
Reactant3-(Hexyloxy)-6-hydroxybenzene-1,2-dicarbonitrileHCID 15006689—
SolventTetrahydrofuranHCID 8028—
Product2,3-Dicyano-4-hexyloxyphenyl 5-hexylthiophene-2-carboxylateHCID 1500669053.4%

Reaction Steps

0.50 g (2.36 mM) of 5-hexylthiophene-2-carboxylic acid (M.W.: 212), 0.58 g (2.36 mM) of 2,3-dicyanohydroquinone monohexyl ether (M.W.: 244) and 20 ml of THF were mixed and stirred. To the mixture, 0.49 g (2.36 mM) of dicyclohexylcarbodiimide (M.W.: 206) and 0.05 g of pyrrolidinopyridine were added, followed by stirring overnight at room temperature. After the reaction, the reaction mixture was subjected to filtration and the filtrate was subjected to distillation to obtain a crude product. The crude product was purified by silica gel column chromatography with the use of benzene and recrystallized from ethanol to obtain 0.55 g of an objective product (yield: 53.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118441
Source datasetuspto-grants-1992_06
ORD IDord-cafb66d079024aa8b5340a302514b76d
Source noteuspto-grants-1992_06