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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356943Generated: November 1, 2026

Phosphate → HCID 13361982, compound

https://huagongshe.com/reaction/1356943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantDibenzyl etherHCID 7657—
ReactantHydroxyacetoneHCID 8299—
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventPalladium hydroxideHCID 9942167—
ProductHCID 13361982HCID 1336198281%

Reaction Steps

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 2111α (39 mg, 0.17 mmol, 32%) in 97% ee. Benzyl ether 2111α (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 1111 (19 mg, 0.14 mmol, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589766B1
Source datasetuspto-grants-2003_07
ORD IDord-40748a05d5e24602b2d915649144e204
Source noteuspto-grants-2003_07