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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403467Generated: October 31, 2026

1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol → 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-one

https://huagongshe.com/reaction/1403467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-olHCID 70665277—
SolventDichloromethaneHCID 6344—
Product1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-oneHCID 1091175880.5%

Reaction Steps

To a solution of 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol (3.0 g, 12.2 mmol) in DCM (50 mL) was added DMP (10.0 g, 24.4 mmol). The resulting solution was stirred for 30 min at room temperature and then the reaction mixture was poured into NaHCO3/NaS2O3 solution and stirred for overnight, extracted with DCM (3×150 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to give a residue. The residue was purified by silica gel column chromatography (3% ethyl acetate in petroleum ether) to afford 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-one as a light yellow oil (2.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-7be7eb5c217e4966b6cd620c7721466e
Source noteuspto-grants-2014_12