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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267988Generated: October 31, 2026

Phosphate → Dibenzyl ether

https://huagongshe.com/reaction/2267988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantHydroxyacetoneHCID 8299—
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
ReactantHCID 13361982HCID 13361982—
SolventAcetonitrileHCID 6342—
ProductDibenzyl etherHCID 765732%

Reaction Steps

FIG. 41 illustrates Ketone 2111a was easily transformed to 1-deoxy-L-xylulose (1111) by hydrogenation. Benzyloxyacetaldehyde (80 mg, 0.53 mmol) in ) in ) 0.5 mL of acetonitrile, was added to 9 mL of a solution of antibody 38C2 (35 mg, 0.23 mmol) in PBS (phosphate buffer saline, 100 mM), followed by the addition of of hydroxyacetone. (0.5 mL, 6.3 mmol). After 48 hr at room temperature the reaction reached 56% conversion and the mixture was freeze dried. The remaining residue was extracted with methylene chloride. The solvent was removed under reduced pressure and the crude product was purified by column chromatography (silica gel, ethyl acetate/hexane, 1/1) to give pure 2111a (39 mg, 0.17 mmol, 32%) in 97% ee. Benzyl ether 2111a (39 mg, 0.17 mmol) was dissolved in 1 mL of methanol and hydrogenated with a catalytic amount of palladium hydroxide on carbon. After two hr, the mixture was filtered through celite and the solvent was removed under reduced pressure to give pure 1-deoxy-L-xylulose (19 mg, 0.14 mmol, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326176B1
Source datasetuspto-grants-2001_12
ORD IDord-c637aa1ef81647d2b15e9e066d535523
Source noteuspto-grants-2001_12