Réaction #84041

ord-b91adc4da59b48229468cf730202c0b0

Équation de réaction

COC(=O)Cl
Methyl chloroformate
[Na+].[OH-]
NaOH
C[C@@H](O)[C@H](N)C(=O)O
L-Threonine
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
COC(=O)N[C@H](C(=O)O)[C@@H](C)O
foam
COC(=O)N[C@H](C(=O)O)[C@@H](C)O
(2S,3R)-3-hydroxy-2-(methoxycarbonylamino)butanoic acid

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrereach room temperature
  2. 2
    LavageThe reaction mixture is washed with CH2Cl2 (3×50 mL)
  3. 3
    Autrethe aqueous layer is contained in a round bottom flask
  4. 4
    Températurecooled over an ice-water bath
  5. 5
    workup.ADDITIONConcentrated HCl (aq) is added drop wise until pH 2
  6. 6
    Autreis brought to room temperature
  7. 7
    Autrethe water is removed in vacuum
  8. 8
    workup.ADDITIONThe residue was taken up in a 2:1 mixture of MeOH/CH2Cl2 (150 mL
  9. 9
    Filtrationfiltered
  10. 10
    Lavagewashed with 2:1 mixture of MeOH/CH2Cl2 (50 mL)
  11. 11
    ConcentrationThe filtrate was concentrated
  12. 12
    Autredried in vacuum at 40° C.

Mode opératoire

An aqueous NaOH (1 M, 167 mL) solution is added, while stirring, to L-Threonine (20 g, 30.5 mmol) in a round bottom flask (1 L). To this solution was added sodium carbonate (9.8 g, 92.3 mmol). The flask is cooled to 0° C. in an ice-water bath. Methyl chloroformate (14.3 mL, 184.7 mmol) is added drop wise and the reaction mixture is allowed to stir for 15 hours and reach room temperature. The reaction mixture is washed with CH2Cl2 (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 aqueous solution is brought to room temperature and the water is removed in vacuum. The residue was taken up in a 2:1 mixture of MeOH/CH2Cl2 (150 mL, filtered and washed with 2:1 mixture of MeOH/CH2Cl2 (50 mL). The filtrate was concentrated and dried in vacuum at 40° C., resulting in white foam (29.1 g, 98%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09433609B2uspto-grants-2016_09