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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625988Generated: November 1, 2026

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

https://huagongshe.com/reaction/1625988

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 numberUS08785438B2
Source datasetuspto-grants-2014_07
ORD IDord-bb0a1ba5a7ab445084a7e78a642fddff
Source noteuspto-grants-2014_07