Reacción #790460

ord-a13823069d3f4c7e8e20d15d32227bcf

Ecuación de reacción

COC(=O)C(CNC(=O)c1ccccc1)C(C)=O
methyl 2-(N-benzoylamino)methyl-3-oxobutanoate
COC(=O)[C@@H](CNC(=O)c1ccccc1)[C@@H](C)O
methyl (2S, 3R)-2-(N-benzoylamino)methyl-3-hydroxybutanoate
Rendimiento 87.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas conducted at 70° C. under a hydrogen
  2. 2
    Otrofor 30 hours
  3. 3
    ConcentraciónThe reaction mixture was concentrated under reduced pressure of 20 mmHg
  4. 4
    Otrothe residue was purified by silica gel column chromatography
  5. 5
    workup.ADDITIONa 7/3 (by volume) mixture of hexane and isopropanol as an eluent

Procedimiento

In a 100 ml-volume stainless steel autoclave whose atmosphere had been displaced with nitrogen was added a solution of 2.5 g (10 mmole) of methyl 2-(N-benzoylamino)methyl-3-oxobutanoate and 184 mg (0.1 mmole) of [Ru((+)BINAP)](CLO4)2 in 18 ml of dichloroethane, and a reaction was conducted at 70° C. under a hydrogen pressure of 100 kg/cm2 for 30 hours. The reaction mixture was concentrated under reduced pressure of 20 mmHg, and the residue was purified by silica gel column chromatography using a 7/3 (by volume) mixture of hexane and isopropanol as an eluent to give 2.19 g (yield: 86.5%) of methyl (2S, 3R)-2-(N-benzoylamino)methyl-3-hydroxybutanoate having an optical purity of 90 %ee.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04981992uspto-grants-1991_01