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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364939Generated: October 26, 2026

Hydrochloric Acid → 1-[4-(1-Imidazolyl)-phenyl]-2-propanone

https://huagongshe.com/reaction/364939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant4-(2-nitro-1-propenyl)phenyl-1H-imidazoleHCID 54001918—
CatalystIronHCID 23925—
SolventDichloromethaneHCID 6344—
Product1-[4-(1-Imidazolyl)-phenyl]-2-propanoneHCID 13394227—

Reaction Steps

A 5.0 liter 3-neck flask fitted with a condenser, addition funnel, and mechanical stirrer is charged with a mixture of 218.4 g (0.954 mole) of 1-[4-(2-nitro-1-propenyl)phenyl-1H-imidazole, 449 g (8.04 mole) of iron powder (325 mesh), 6.4 g of FeCl3 6H2O, 350 ml of methanol and 760 ml of water. The mixture is heated to reflux with stirring and 450 ml of concentrated hydrochloric acid is added dropwise over a period of 2.5 hours. Refluxing is continued for two to three hours. The reaction mixture is cooled to room temperature, 1.9 liter of CH2Cl2 was added, and the mixture stirred rapidly for one hour. This is filtered, the inorganic solid is washed three times with 500 ml portions of CH2Cl2, and the layers separated. The CH2Cl2 layer is dried over MgSO4, then filtered through a bed of silica gel (600 g, 70-230 mesh), which is washed with 5 liters of CH2Cl2 and then with 13 liters of 10% methanol in methylene chloride. Evaporation of the solvent gave 126.7 g of a brown oil which crystallized on standing. The product is purified via the sodium bisulfate addition product to give a product having a mp of 71.5°-72.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04607037
Source datasetuspto-grants-1986_08
ORD IDord-0b054530ea55477b844bf4f2bfdc8991
Source noteuspto-grants-1986_08