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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104227Generated: October 30, 2026

Hydrogen Peroxide → Tetrahydro-3'R,5'R-dibenzoyloxy-6'S-methyl-2H-pyrane

https://huagongshe.com/reaction/2104227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant(2S,3R,5R)-2-methyl-6-oxotetrahydro-2H-pyran-3,5-diyl dibenzoateHCID 11473679—
ReactantDiisoamylborohydrideHCID 131727586—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTetrahydro-3'R,5'R-dibenzoyloxy-6'S-methyl-2H-pyraneHCID 1606647893.9%

Reaction Steps

The compound (IX) (5 g, 14.11 mmol) dissolved in dry THF (15 ml) is added to 0.5M Diisoamylborohydride (127 ml) prepared in the reaction (1). Then, it is stirred for 20 hours at a room temperature. After the reaction is finished, water (3 ml) is added and then stirred for 30 minutes. The reaction mixture is cooled to 0° C., and then 30% H2O2 (15 ml) is added and 3N NaOH is added to maintain the pH 7-8. The solvent THF is vacuum concentrated, and then it is dissolved in CH2Cl2 (100 ml) and washed by water (50 ml). An organic layer is dried using anhydrous MgSO4. The solution is vacuum concentrated, and then the compound (II) (4.72 g, 93.8%, α:β=4.6:1) is isolated using flash column chromatography (toluene/EtOAc, 10:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576225B2
Source datasetuspto-grants-2009_08
ORD IDord-a6ab7491b1bc4565b276836679538df4
Source noteuspto-grants-2009_08