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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458763Generated: October 29, 2026

Sodium Sulfite → HCID 69075646, compound

https://huagongshe.com/reaction/458763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantHCID 69073653HCID 69073653—
CatalystOsmium TetroxideHCID 30318—
SolventEthyl AcetateHCID 8857—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 69075646HCID 69075646—

Reaction Steps

To a solution of 69 mg of the t-butyl 4-((2R)-2-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-vinylphenyl)ethanoyloxy)-tetrahydropyridine-1(2H)-carboxylate as obtained in Referential Example 56 in 2 ml of tetrahydrofuran-water (1:1), 85 mg of sodium periodide and 0.1 ml of 2% osmium tetraoxide were added at 0° C., followed by an hour's stirring at the same temperature. Adding sodium sulfite to the reaction liquid, stirring was continued for further 30 minutes. The reaction liquid was diluted with ethyl acetate, washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the residue was dissolved in 1 ml of methanol. To the solution 10 mg of sodium borohydride was added, stirred for 10 minutes and acetone was added. The reaction liquid was diluted with ethyl acetate, washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the resulting residue was purified on preparative thin layer chromatography (Kieselgel™ 60F254, Art 5744 (Merck), hexane/ethyl acetate=1/1) to provide 42 mg of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192969B2
Source datasetuspto-grants-2007_03
ORD IDord-a60fe93f3b9f4d6ba11b7380e3b7b660
Source noteuspto-grants-2007_03