Reaktion #1065129

Reaktionsgleichung

Sodium hydride

3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine

benzyl bromide

→

1-benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine

Ausbeute 62.0%

Lösungsmittel

N,N-dimethylformamide

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture is further stirred for 1 hour
2. 2
   SonstigeAfter the reaction
3. 3
   workup.DISTILLATIONthe reaction mixture is distilled
4. 4
   Sonstigeto remove the solvent under reduced pressure
5. 5
   workup.DISSOLUTIONthe residue is dissolved in chloroform
6. 6
   WaschenThe chloroform solution is washed with an aqueous saturated sodium chloride solution
7. 7
   Sonstigedried
8. 8
   workup.DISTILLATIONdistilled
9. 9
   Sonstigeto remove the solvent
10. 10
    SonstigeThe residue is recrystallized from isopropyl alcohol

Vorschrift

Sodium hydride (60% dispersion in oil) (47 mg) is suspended in N,N-dimethylformamide (2 ml), and to the suspension is added dropwise a solution of 3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine (200 mg) in N,N-dimethylformamide (16 ml). The mixture is stirred for 10 minutes and thereto is added benzyl bromide (0.12 ml), and the mixture is further stirred for 1 hour. After the reaction, the reaction mixture is distilled to remove the solvent under reduced pressure and the residue is dissolved in chloroform. The chloroform solution is washed with an aqueous saturated sodium chloride solution, dried and then distilled to remove the solvent. The residue is recrystallized from isopropyl alcohol to give 1-benzyl-3-(1,3-dithiol-2-ylidene)-2,4-dioxopiperidine (176 mg, 62%) as pale yellow needles. m.p. 122°-124° C.

Quelle