Реакция #84040

ord-39ad65ac9fc142649a7bb14dd4f1e092

Уравнение реакции

COC(=O)Cl
Methyl chloroformate
[Na+].[OH-]
NaOH
CC(C)C[C@H](N)C(=O)O
L-Leucine
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
COC(=O)N[C@@H](CC(C)C)C(=O)O
(S)-2-(methoxycarbonylamino)-4-methylpentanoic acid

Реагенты

Нет

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеreach room temperature
  2. 2
    ДругоеThe reaction mixture is separated with ether (3×50 mL)
  3. 3
    Другоеthe aqueous layer is contained in a round bottom flask
  4. 4
    Температураcooled over an ice-water bath
  5. 5
    workup.ADDITIONConcentrated HCl (aq) is added drop wise until pH 2
  6. 6
    Другоеis brought to room temperature
  7. 7
    Экстракцияextracted with 2-Me-THF (3×50 mL)
  8. 8
    Сушкаdried (MgSO4)
  9. 9
    Другоеthe solids removed by filtration
  10. 10
    Другоеthe solvents of the filtrate removed under reduced pressure
  11. 11
    ДругоеThe compound was purified by silicagel chromatography with gradient elution from CH2Cl2 to CH2Cl2/MeOH/acetic acid 17/2/1
  12. 12
    workup.ADDITIONFractions containing product
  13. 13
    Другоеthe solvent were removed in vacuum
  14. 14
    Другоеresulting in N-methoxycarbonyl-L-leucine (1.9 g, 32%)

Методика

An aqueous NaOH (1M, 2.6 mL) solution is added, while stirring, to L-Leucine (4 g, 30.5 mmol) in a round bottom flask (250 mL). To this solution was added sodium carbonate (1.62 g, 15.2 mmol). The flask is cooled to 0° C. in an ice-water bath. Methyl chloroformate (2.6 mL, 33.5 mmol) is added drop wise and the reaction mixture is allowed to stir for 15 hours and reach room temperature. The reaction mixture is separated with ether (3×50 mL), and the aqueous layer is contained in a round bottom flask and cooled over an ice-water bath. Concentrated HCl (aq) is added drop wise until pH 2. The reaction mixture is brought to room temperature and extracted with 2-Me-THF (3×50 mL). The organic layers are pooled, dried (MgSO4), the solids removed by filtration, and the solvents of the filtrate removed under reduced pressure. The compound was purified by silicagel chromatography with gradient elution from CH2Cl2 to CH2Cl2/MeOH/acetic acid 17/2/1. Fractions containing product were combined and the solvent were removed in vacuum, resulting in N-methoxycarbonyl-L-leucine (1.9 g, 32%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09433609B2uspto-grants-2016_09