Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569895Generated: October 29, 2026

Ethyl formate → HCID 67870812, compound

https://huagongshe.com/reaction/569895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantSodium hydrideHCID 24758—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
CatalystEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67870812HCID 67870812—

Reaction Steps

1,4-Cyclohexanedione monoethylene ketal (5.00 g) was added to a mixture of sodium hydride (1.40 g of a 60% suspension in mineral oil), 10 ml of ethyl formate, 1 drop of ethanol and 200 ml of tetrahydrofuran. The reaction mixture was heated at reflux for 2.5 hours, cooled and partitioned between water and ethyl ether. The ethereal layer was extracted several times with 0.5N sodium hydroxide and the combined aqueous portions were washed once with ether. The aqueous solution was acidified slowly to a pH of 4 with 5N hydrochloric acid and the slurry was exhaustively extracted with dichloromethane. The combined extracts were dried over magnesium sulfate and concentrated in vacuo to provide a dark oil. The oil was distilled bulb-to-bulb (120° C./lmm) to afford 7-(hydroxymethylene)-1,4-dioxaspiro-[4.5]decan-8-one as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734429
Source datasetuspto-grants-1988_03
ORD IDord-ead8602fd2db4450baefd45de479dd26
Source noteuspto-grants-1988_03