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HRID 46639생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dimethyl-2-imidazolidinoneHCID 6661—
반응물BenzhydrylamineHCID 7036—
반응물Sodium HydroxideHCID 14798—
용매DichloromethaneHCID 6344—
생성물1,3-Dimethyl-2-diphenylmethyliminoimidazolidineHCID 12503418—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04174401
출처 데이터셋uspto-grants-1979_11
ORD IDord-00fd6391401b42e9bb00c6cfd759d940
출처 메모uspto-grants-1979_11