Reacción #155405

ord-05547141b5f2496c85acf69650ed38b3

Ecuación de reacción

CC(C)(C)OC(=O)N1CC(=O)C1
N-Boc-3-azetidinone
CC(C)(C)OC(=O)[CH2][Zn+].[Cl-]
2-tert-butoxy-2-oxoethyl-zinc chloride
CCOCC
Et2O
CC(C)(C)OC(=O)CC1(O)CN(C(=O)OC(C)(C)C)C1
tert-butyl-2-(N-Boc-3-hydroxy-azetidin-3-yl)-acetate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction was then quenched with sat. aq. NH4Cl (10 mL)
  2. 2
    Otrothe aqueous layer was separated
  3. 3
    Extracciónextracted with ethyl acetate (2×30 mL)
  4. 4
    LavadoThe combined organic layers were washed with 5% aq. NaHCO3 (2×10 mL), brine (15 mL)
  5. 5
    Secadodried over Na2SO4
  6. 6
    Filtraciónfiltered
  7. 7
    Concentraciónconcentrated to dryness

Procedimiento

To a stirring solution of N-Boc-3-azetidinone (0.45 g, 2.64 mmol) in THF (5 mL) was slowly added a 0.5 M solution of 2-tert-butoxy-2-oxoethyl-zinc chloride in Et2O (10 mL, 5.0 mmol), and the reaction mixture was stirred for 5 h. The reaction was then quenched with sat. aq. NH4Cl (10 mL), and the aqueous layer was separated and extracted with ethyl acetate (2×30 mL). The combined organic layers were washed with 5% aq. NaHCO3 (2×10 mL), brine (15 mL), dried over Na2SO4, filtered and concentrated to dryness to yield tert-butyl-2-(N-Boc-3-hydroxy-azetidin-3-yl)-acetate (MS m/e [M+H]+ calcd 288.2. found 287.7).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822424B2uspto-grants-2014_09