反応 #70973

反応方程式

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

溶媒

1,4-dioxane

1,4-dioxane

反応条件

後処理

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

実験手順

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.

出典