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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225114Generated: October 25, 2026

1,3-Dimethyl-2-imidazolidinone → 1,3-Dimethyl-2-diphenylmethyliminoimidazolidine

https://huagongshe.com/reaction/225114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantBenzhydrylamineHCID 7036—
ReactantSodium HydroxideHCID 14798—
SolventDichloromethaneHCID 6344—
Product1,3-Dimethyl-2-diphenylmethyliminoimidazolidineHCID 12503418—

Reaction Steps

To 3.79 grams (0.027 mole) of boron trifluoride etherate in 3 milliliters of anhydrous ether under dry argon, is added as rapidly as possible while maintaining control of the reaction, 1.8 gram (0.02 mole) of epichlorohydrin in 7 milliliters of dry ether. After about 3 hours, the crystals of triethyloxonium fluoborate which are formed are separated and washed with fresh dry ether under dry argon. The crystals are then dissolved in dry methylene chloride (5 ml.) and a solution of 2.28 grams (0.02 mole) of 1,3-dimethyl-2-imidazolidinone in 25 milliliters of dry methylene chloride is added. After stirring at room temperature for about 3 hours, 3.66 gram (0.02 mole) of benzhydrylamine in 5 milliliters of methylene chloride is added. The resulting mixture is allowed to stir overnight at room temperature. Treatment of the reaction mixture with excess cold (0° C.) 20% NaOH, shaking, and separation of the organic layer gives a solution of the free base. This solution is dried over anhydrous potassium carbonate, filtered and the solvent is vaporized in vacuo to afford the 1,3-dimethyl-2-diphenylmethyliminoimidazolidine product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235894
Source datasetuspto-grants-1980_11
ORD IDord-b2801b82f3694bbfa709b4eef97f3d22
Source noteuspto-grants-1980_11