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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant(2R,3S)-2-methyl-3-benzyloxybutanolHCID 11252551—
SolventDimethyl SulfoxideHCID 679—
Product(2S,3S)-2-methyl-3-benzyloxybutyraldehydeHCID 86590269—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432087B2
Source datasetuspto-grants-2008_10
ORD IDord-16ceb8de43154b8a8be6c824805cd3d5
Source noteuspto-grants-2008_10