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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28307Generated: October 23, 2026

Hydrochloric Acid → 2-(2-Methyl-5-nitroimidazolyl)ethyl-z,z-octadeca-9,12-dienoate

https://huagongshe.com/en/reaction/28307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMetronidazoleHCID 4173—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantLinoleic AcidHCID 5280450—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-(2-Methyl-5-nitroimidazolyl)ethyl-z,z-octadeca-9,12-dienoateHCID 136388346—

Reaction Steps

To a suspension of metronidazole (1.9 g) in dry dichloromethane (20 ml) was added successively 4-(N,N-dimethylamino)pyridine (1.22 g), 1,3-dicyclohexylcarbodiimide (2.2 g) and linoleic acid (2.8 g). The mixture was stirred at room temperature overnight. To the reaction was added 2M hydrochloric acid (20 ml) and stirring was continued. After filtration the organic layer was separated, washed with 50% saturated brine and finally with saturated aqueous sodium bicarbonate. The dichloromethane solution was dried (sodium sulfate) and evaporated in vacuo (30° C./20 mm Hg). To the resulting residue was added petrol (bp 30-60° C., 20 ml) and the mixture allowed to stand at room temperature for 2 hours, causing the precipitation of the remaining urea. This was removed by filtration and the filtrate was applied to a dry column giving 2-(2-methyl-5-nitroimidazolyl)ethyl-z,z-octadeca-9,12-dienoate as a pale yellow, non distillable oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE040480E1
Source datasetuspto-grants-2008_09
ORD IDord-2eedaae621664893aefd23c02cc0d4a6
Source noteuspto-grants-2008_09