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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121307Generated: October 26, 2026

Dicyclohexylcarbodiimide → 2-[(E)-hex-2-enoyloxy]-5-(4'-hexylbiphenyl-4-yl)thiophene

https://huagongshe.com/reaction/2121307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Hexenoic acid, (2E)-HCID 5282707—
Reactant2-Hydroxy-5-(4'-hexylbiphenyl-4-yl)thiopheneHCID 23432173—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-[(E)-hex-2-enoyloxy]-5-(4'-hexylbiphenyl-4-yl)thiopheneHCID 2343218449.8%

Reaction Steps

Dicyclohexylcarbodiimide (0.4 g) is added to a solution of 2-hydroxy-5-(4′-hexylbiphenyl-4-yl)thiophene (0.25 g), (E)-hex-2-enoic acid, (0.2 g) 4-(dimethylamino)pyridine (0.10 g) and dichloromethane (50 cm3) at 0° C. under an atmosphere of nitrogen. The reaction mixture is stirred overnight at room temperature, filtered to remove inorganic material and the filtrate evaporated down. The residue is purified by column chromatography on silica gel using hexanelethyl acetate (9/1 v/v) as eluent and recrystallisation from hexane to yield 0.16 g of 2-[(E)-hex-2-enoyloxy]-5-(4′-hexylbiphenyl-4-yl)thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696110B1
Source datasetuspto-grants-2004_02
ORD IDord-d1994db4896a418391c015b7f5dd9ecf
Source noteuspto-grants-2004_02