Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516887Generated: October 30, 2026

Benzyl 2-hydroxy-2-(tetrahydro-2H-pyran-4-yl)acetate → Benzyl 2-oxo-2-(tetrahydro-2H-pyran-4-yl)acetate

https://huagongshe.com/reaction/516887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 2-hydroxy-2-(tetrahydro-2H-pyran-4-yl)acetateHCID 90185045—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-oxo-2-(tetrahydro-2H-pyran-4-yl)acetateHCID 9018497990%

Reaction Steps

A Dess-Martinn reagent (5.7 g, 13.44 mmol) was added to a solution of benzyl 2-hydroxy-2-(tetrahydro-2H-pyran-4-yl)acetate (2.1 g, 8.404 mmol) in dichloromethane (50 ml) at room temperature, and the mixture was stirred for 15 hr. The reaction mixture was quenched with 10% sodium thiosulfate and was extracted with dichloromethane. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and saturated brine and was dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was chromatographed on silica gel column (hexane:ethyl acetate=9:1) to give the title compound as a light yellow oil (1.8 g, yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115079B2
Source datasetuspto-grants-2015_08
ORD IDord-0f5f6ed958ac4c1c963522207fc6ebc9
Source noteuspto-grants-2015_08