Water → (2S,3S)-2-methyl-3-benzyloxybutyraldehyde

HRID 2113403Notes

Reaction equation

HRID 2113403 reaction equation
[CH3:1][C@@H:2]([C@@H:5]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:6])[CH2:3][OH:4].CCN(CC)CC.O.CCOCC>CS(C)=O>[CH3:1][C@@H:2]([C@@H:5]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:6])[CH:3]=[O:4]

Participants

6

Conditions

Temperature
0 °C

Procedure

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).

Workup

  1. waitat room temperature for 2 hours
  2. extractionThe aqueous layer was extracted with ether
  3. washThe combined ether extracts were washed with 1M HCl, waters saturated NaHCO3, brine, and they
  4. dry with materialwere dried over Na2SO4
  5. customevaporated in order

Sources & evidence

ORD record
ord-16ceb8de43154b8a8be6c824805cd3d5
Source dataset
uspto-grants-2008_10
Patent number
US07432087B2

Reaction notes

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