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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716116Generated: October 30, 2026

Glyoxylic Acid → (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal

https://huagongshe.com/reaction/716116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxylic AcidHCID 760—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant(2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal O-methyloximeHCID 131734111—
SolventTetrahydrofuranHCID 8028—
Product(2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanalHCID 118108771—

Reaction Conditions

Temperature70 °C

Reaction Steps

3.3 mL of a 50% glyoxylic acid aqueous solution was added to a solution of 662 mg of the (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal O-methyloxime in 6.6 mL of tetrahydrofuran, and the obtained mixture was then stirred at 70° C. for 4.83 hours. Thereafter, ethyl acetate and water were added to the reaction mixture. The organic layer was fractionated, and it was washed with a sodium hydrogen carbonate aqueous solution, and was then dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, so as to obtain 655 mg of colorless oily (2S,3S,4S)-4-bromo-2-fluoro-3,5-bis(benzyloxy)pentanal and a water adduct thereof.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187514B2
Source datasetuspto-grants-2015_11
ORD IDord-77bc70c6d0b245059c0a55710e1fa2c0
Source noteuspto-grants-2015_11