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HRID 46639作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/46639

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Dimethyl-2-imidazolidinoneHCID 6661—
反応物BenzhydrylamineHCID 7036—
反応物Sodium HydroxideHCID 14798—
溶媒DichloromethaneHCID 6344—
生成物1,3-Dimethyl-2-diphenylmethyliminoimidazolidineHCID 12503418—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04174401
出典データセットuspto-grants-1979_11
ORD IDord-00fd6391401b42e9bb00c6cfd759d940
出典メモuspto-grants-1979_11