反応 #1328409

反応方程式

7-butyryloxy-3-benzyloxycarbonylmethylaminocarbonyl-6-chlorocoumarin

hydrogen

hydrogen

acetic acid

coumarin

coumarin

coumarin

→

7-Butyryloxy-3-carboxymethylaminocarbonyl-6-chlorocoumarin

溶媒

dioxane

反応条件

後処理

1. 1
   ろ過was filtered
2. 2
   workup.ADDITIONThe product containing carbon
3. 3
   抽出was extracted five times with 25 ml
4. 4
   温度to cool upon which the product
5. 5
   その他precipitated as a white powder
6. 6
   その他Reduction of the solvent to 20 ml precipitates more product
7. 7
   温度The remaining dioxane solution is heated
8. 8
   workup.ADDITIONheptane is added until the solution

実験手順

7-Butyryloxy-3-carboxymethylaminocarbonyl-6-chlorocoumarin was prepared as follows. 920 mg (2 mMol) 7-butyryloxy-3-benzyloxycarbonylmethylaminocarbonyl-6-chlorocoumarin were dissolved in 50 ml dioxane. 100 mg palladium on carbon (10%) and 100 microliters acetic acid were added to the solution and the suspension stirred vigorously in a hydrogen atmosphere at ambient pressure. After the uptake of hydrogen seized the suspension was filtered. The product containing carbon was extracted five times with 25 ml boiling dioxane. The combined dioxane solutions were let to cool upon which the product precipitated as a white powder. Reduction of the solvent to 20 ml precipitates more product. The remaining dioxane solution is heated to boiling and heptane is added until the solution becomes cloudy. The weights of the dried powders were 245 mg, 389 mg and 58 mg, totaling 692 mg (1.88 mMol, 94%) of white product. 1H NMR (dDMSO): δ 1.02 ppm (t, 3H, J=7.4 Hz, butyric methyl), δ 1.73 ppm (m, 2H, J1≈J2=7.3 Hz, butyric methylene), δ 2.70 ppm (t, 2H, J=7.2 Hz, butyric methylene), δ 4.07 ppm (d, 2H, J=5.6 Hz, glycine methylene), δ 7.67 ppm (s, 1H, coumarin), δ 8.35 ppm (s, 1H, coumarin), δ 8.90 ppm (s, 1H, coumarin), δ 9.00 ppm (t, 1H, J=5.6 Hz, amide).

出典