Reaktion #74917

Reaktionsgleichung

1,3-dimethyl-2-imidazolidinone

benzhydrylamine

NaOH

→

1,3-dimethyl-2-diphenylmethyliminoimidazolidine

Lösungsmittel

methylene chloride

methylene chloride

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeare separated
2. 2
   Waschenwashed with fresh dry ether under dry argon
3. 3
   workup.DISSOLUTIONThe crystals are then dissolved in dry methylene chloride (5 ml.)
4. 4
   workup.STIRRINGto stir overnight at room temperature
5. 5
   Sonstigeseparation of the organic layer
6. 6
   Sonstigegives a solution of the free base
7. 7
   TrocknenThis solution is dried over anhydrous potassium carbonate
8. 8
   Filtrationfiltered

Vorschrift

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.

Quelle