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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088953Generated: November 3, 2026

Water → Ethyl 2-(oxan-4-ylidene)acetate

https://huagongshe.com/reaction/2088953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 2-(oxan-4-ylidene)acetateHCID 11105795—
ProductHCID 22965801HCID 22965801—

Reaction Steps

55% Sodium hydride (2.6 g) was suspended in dimethoxyethane (150 ml). Ethyl diethylphosphonoacetate (9.6 ml) was added dropwise under nitrogen atmosphere under ice-cooling over five minutes, and the mixture was stirred at the same temperature for 45 minutes. A solution of tetrahydro-4H-pyran-4-one (4.0 g) in dimethoxyethane (10 ml) was added dropwise thereto over five minutes. The mixture was stirred at room temperature for 10 minutes and then heated under reflux for one hour. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (developed with ethyl acetate-hexane) to give the title compounds ethyl tetrahydro-4H-pyran-4-ylideneacetate (1.7 g) and ethyl 3,6-dihydro-2H-pyran-4-ylacetate (2.2 g) both as colorless oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436012B2
Source datasetuspto-grants-2013_05
ORD IDord-e1f9540bbd1341868e866358b53d659b
Source noteuspto-grants-2013_05