反応 #93016

反応方程式

16β-ethyl-17β-bromoacetoxy-4-estren-3-one

N-t-butoxycarbonylleucine

potassium t-butoxide

water

→

above-identified compound

収率 80.5%

16β-Ethyl-17β-(N-t-butoxycarbonylleucyl)oxyacetoxy-4-estren-3-one

収率 80.5%

溶媒

acetone

反応条件

後処理

1. 1
   workup.ADDITIONare added
2. 2
   温度The mixture is refluxed for 12 hours
3. 3
   workup.DISTILLATIONThe solvent is then distilled off under reduced pressure
4. 4
   抽出the residue is extracted with 150 ml of ethyl acetate
5. 5
   その他The organic layer is separated
6. 6
   洗浄washed with water and saturated aqueous sodium chloride solution
7. 7
   乾燥dried over anhydrous magnesium sulfate
8. 8
   workup.DISTILLATIONThe solvent is distilled off under reduced pressure
9. 9
   洗浄After serial passage of diisopropyl ether-n-hexane mixtures (1:3, 400 ml and 5:2, 750 ml), elution
10. 10
    workup.ADDITIONis carried out with 1000 ml of a 4:1 mixture of the same solvents
11. 11
    その他The eluate is evaporated under reduced pressure
12. 12
    その他to remove the solvent

実験手順

In 40 ml of acetone is dissolved 1.2 g of N-t-butoxycarbonylleucine, and 1.2 g of potassium t-butoxide and 8 ml of water are added, followed by addition of 1.1 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one. The mixture is refluxed for 12 hours. The solvent is then distilled off under reduced pressure and the residue is extracted with 150 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is distilled off under reduced pressure and the residue is subjected to column chromatography. After serial passage of diisopropyl ether-n-hexane mixtures (1:3, 400 ml and 5:2, 750 ml), elution is carried out with 1000 ml of a 4:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.2 g of the above-identified compound as a colorless viscous oil.

出典