HRID6067

反应详情

EQUATION

反应方程式

HRID 6067 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

565 mg of N-[(benzyloxy)carbonyl]-L-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2-oxetanyl]methyl]octadecyl ester were dissolved in 12 ml of THF. The mixture was hydrogenated at room temperature in the presence of 40 mg of 10% Pd/C. After the reaction was finished the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in 9 ml of THF and 71 μl of formic acid/acetic acid anhydride were added dropwise. The mixture was diluted with 5 ml of diethyl ether and washed twice with 2% sodium hydrogen carbonate solution and then with water. After drying over sodium sulfate it was filtered and evaporated. By chromatography on silica gel and recrystallization from n-pentane there was obtained N-formyl-(S)-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2-oxetanyl]methyl]octadecyl ester of m.p. 60°-61° C.

WORKUP

后处理

  1. filtrationwas filtered off
  2. customthe filtrate was evaporated
  3. addition71 μl of formic acid/acetic acid anhydride were added dropwise
  4. additionThe mixture was diluted with 5 ml of diethyl ether
  5. washwashed twice with 2% sodium hydrogen carbonate solution
  6. dry with materialAfter drying over sodium sulfate it
  7. filtrationwas filtered
  8. customevaporated
  9. customBy chromatography on silica gel and recrystallization from n-pentane