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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457383Generated: October 30, 2026

Potassium Carbonate → HCID 18437793, compound

https://huagongshe.com/reaction/457383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
ReactantBenzo-1,3-dioxole-5-methylamineHCID 75799—
ReactantHCID 18437794HCID 18437794—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 18437793HCID 18437793—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Butyl-5-hydroxymethyl-2-iodo-4-phenylimidazole (1.96 g, 6.1 mmol) is dissolved in 20 ml dichloromethane and cooled to 0° C. To the solution is added 5 equivalents of thionyl chloride and the resulting solution is stirred at room temperature for 2 h. The reaction mixture is evaporated at reduced pressure and 20 ml of toluene is added to the residue and evaporated to remove any residual thionyl chloride. The crude product is dissolved in 20 ml of anhydrous acetonitrile and added to an ice-cooled solution of piperonyl amine (2.0 eq.) in acetonitrile (10 mL) containing potassium carbonate (2 eq.). The resulting mixture is stirred at room temperature for 4 h, diluted with 100 ml of ethyl acetate, washed with water and brine, dried over sodium sulfate and concentrated at reduced pressure. The residue is purified by silica gel chromatography (hexanes/ethyl acetate, from 2:1 to 1:1) to give 2.28 g of 1-butyl-5-chloromethyl-2-iodo-4-phenylimidazole. MS (+VE) m/z 490 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186734B2
Source datasetuspto-grants-2007_03
ORD IDord-5a3d750599ad4a22be2c1520ccae0f1a
Source noteuspto-grants-2007_03