Reacción #2200585

ord-16ceb8de43154b8a8be6c824805cd3d5

Ecuación de reacción

O
water
C[C@H](CO)[C@H](C)OCc1ccccc1
(2R,3S)-2-methyl-3-benzyloxybutanol
CCN(CC)CC
Et3N
CCOCC
ether
C[C@H](C=O)[C@H](C)OCc1ccccc1
(2S,3S)-2-methyl-3-benzyloxybutyraldehyde

Disolventes

Condiciones de reacción

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

Tratamiento posterior

  1. 1
    workup.WAITat room temperature for 2 hours
  2. 2
    ExtracciónThe aqueous layer was extracted with ether
  3. 3
    LavadoThe combined ether extracts were washed with 1M HCl, waters saturated NaHCO3, brine, and they
  4. 4
    Secadowere dried over Na2SO4
  5. 5
    Otroevaporated in order

Procedimiento

The Py.SO3 complex (4.09 g, 25.67 mmol, 6.0 eq.) was added in portions at 0° C. to a solution of (2R,3S)-2-methyl-3-benzyloxybutanol (13) (830 mg, 4.28 mmol) and Et3N (2.86 g, 3.93 ml, 28.25 mmol, 6.6 eq.) in DMSO (14 ml). The reaction mixture is stirred at 0° C. for 3.5 hours, and then at room temperature for 2 hours, and then it was divided between water and ether. The aqueous layer was extracted with ether. The combined ether extracts were washed with 1M HCl, waters saturated NaHCO3, brine, and they were dried over Na2SO4 and evaporated in order to obtain crude (2S,3S)-2-methyl-3-benzyloxybutyraldehyde which was used directly for the next reaction without purification. 1H NMR (250 MHz, CDCl3) δ 9.73 (d, J=2.4 Hz, 1H); 4.63 (d, J=11.7 Hz, 1H); 4.44 (d, J=11.7 Hz, 1H); 3.81 (quintuplet, J=6.4 Hz, 1H); 2.57 (quintuplet-d, J=7.0; 2.4 Hz, 1H); 1.25 (d, J=6.2 Hz, 3H); 1.09 (d, J=7.1 Hz, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07432087B2uspto-grants-2008_10