HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113403Generated: October 29, 2026
Water → (2S,3S)-2-methyl-3-benzyloxybutyraldehyde
https://huagongshe.com/reaction/2113403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2R,3S)-2-methyl-3-benzyloxybutanol | HCID 11252551 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (2S,3S)-2-methyl-3-benzyloxybutyraldehyde | HCID 86590269 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432087B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-16ceb8de43154b8a8be6c824805cd3d5 |
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| Source note | uspto-grants-2008_10 |
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