반응 #2200585

ord-16ceb8de43154b8a8be6c824805cd3d5

반응 방정식

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

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07432087B2uspto-grants-2008_10