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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606973Generated: October 30, 2026

Hydrogen Peroxide → Trans-6-benzhydryl-tetrahydropyran-3-ol

https://huagongshe.com/reaction/606973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant2-benzhydryl-3,4-dihydro-2H-pyranHCID 66631227—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductTrans-6-benzhydryl-tetrahydropyran-3-olHCID 1160869793.5%

Reaction Steps

Into a solution of 0.5M 9-BBN-THF complex (24 ml, 12 mmol) in dry THF (20 ml) was added in a drop wise manner 2-diphenyl-3,4-dihydro-2H-pyran 10 (1 g, 4 mmol) dissolved in dry THF (10 ml). The mixture was kept under stirring at room temperature. After the completion of initial addition reaction, the intermediate reaction mixture was oxidized with 5.3 ml 3N sodium hydroxide and 3 ml of 30% hydrogen peroxide. The reaction was continued at 55° C. for 1 hr to insure the completion of oxidation. After the mixture was diluted with sat. aqueous NaHCO3, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3×40 ml). The combined extract was dried over anhydrous Na2SO4. The solvent was removed in vacuo and the crude product was purified by flash chromatography (Hexane/Ethyl Acetate 7:3) to furnish trans-6-diphenyltetrahydropyran-3-ol 11 (1 g, 93.5%) as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915433B2
Source datasetuspto-grants-2011_03
ORD IDord-7685bfeb9d2a4e82b4e817836f85f5cd
Source noteuspto-grants-2011_03