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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-benzhydryl-3,4-dihydro-2H-pyran | HCID 66631227 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Trans-6-benzhydryl-tetrahydropyran-3-ol | HCID 11608697 | 93.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915433B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-7685bfeb9d2a4e82b4e817836f85f5cd |
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| Source note | uspto-grants-2011_03 |
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