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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121301Generated: November 3, 2026

Dicyclohexylcarbodiimide → 2-(4-[(E)-hex-2-enoyloxy]phenyl)-5-octylthiazole

https://huagongshe.com/reaction/2121301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Hexenoic acid, (2E)-HCID 5282707—
Reactant2-(4-Hydroxyphenyl)-5-octylthiazoleHCID 135844842—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-(4-[(E)-hex-2-enoyloxy]phenyl)-5-octylthiazoleHCID 2343206045%

Reaction Steps

Dicyclohexylcarbodiimide (0.2 g) is added to a solution of 2-(4-hydroxyphenyl)-5-octylthiazole (0.25 g), (E)-hex-2-enoic acid, (0.1 g) 4-(dimethylamino)pyridine (0.05 g) and dichloromethane (20 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 hexane/ethyl acetate (9/1 v/v) as eluent and recrystallisation from hexane to yield 0.15 g of 2-(4-[(E)-hex-2-enoyloxy]phenyl)-5-octylthiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696110B1
Source datasetuspto-grants-2004_02
ORD IDord-a84420e1b3934a5d9c3dd9d84675595e
Source noteuspto-grants-2004_02