تفاعل #2200585

ord-16ceb8de43154b8a8be6c824805cd3d5

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07432087B2uspto-grants-2008_10