Reaktion #70973

Reaktionsgleichung

6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde

propane-1-thiol

NaH

→

1,3-Dimethyl-2,4-dioxo-6-(propylthio)-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde

Lösungsmittel

1,4-dioxane

1,4-dioxane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewas consumed (monitored by TLC)
2. 2
   workup.ADDITIONThen the mixture was poured onto ice water (50 ml)
3. 3
   Extraktionthe aqueous phase was extracted with ethyl acetate (3×30 ml)
4. 4
   WaschenThe combined organic phases were washed with water
5. 5
   Trocknendried over anhydrous MgSO4
6. 6
   SonstigeThe solvent was evaporated in vacuo
7. 7
   Sonstigethe crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent

Vorschrift

To a stirred solution of propane-1-thiol (2.30 mmol) in dry 1,4-dioxane (4 ml), NaH (2.30 mmol) was added under argon. To the mixture, a solution of 6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (2 mmol) in dry 1,4-dioxane (8 ml) was added at 5-8° C. in one portion. The mixture was stirred at room temperature until the starting material was consumed (monitored by TLC). Then the mixture was poured onto ice water (50 ml) and the aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phases were washed with water and dried over anhydrous MgSO4. The solvent was evaporated in vacuo and the crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent.

Quelle