Reacción #84040

ord-39ad65ac9fc142649a7bb14dd4f1e092

Ecuación de reacción

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

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroreach room temperature
  2. 2
    OtroThe reaction mixture is separated with ether (3×50 mL)
  3. 3
    Otrothe aqueous layer is contained in a round bottom flask
  4. 4
    Temperaturacooled over an ice-water bath
  5. 5
    workup.ADDITIONConcentrated HCl (aq) is added drop wise until pH 2
  6. 6
    Otrois brought to room temperature
  7. 7
    Extracciónextracted with 2-Me-THF (3×50 mL)
  8. 8
    Secadodried (MgSO4)
  9. 9
    Otrothe solids removed by filtration
  10. 10
    Otrothe solvents of the filtrate removed under reduced pressure
  11. 11
    OtroThe 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
    Otrothe solvent were removed in vacuum
  14. 14
    Otroresulting in N-methoxycarbonyl-L-leucine (1.9 g, 32%)

Procedimiento

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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09433609B2uspto-grants-2016_09