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HRID 639552Erstellt: 27. Oktober 2026

Cycloate → 6-Methoxy-1-oxaspiro[2,5]octane

https://huagongshe.com/reaction/639552

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCycloateHCID 14337—
EduktSodium hydrideHCID 24758—
EduktSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
Edukt4-MethoxycyclohexanoneHCID 535028—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt6-Methoxy-1-oxaspiro[2,5]octaneHCID 15329490—

Reaktionsschritte

To a stirred suspension of sodium hydride (60% in mineral oil, 1.20 g, 30.0 mmol) in dimethylsulfoxide (19 mL) was added trimethylsulfoxonium iodide (6.89 g, 31.3 mmol) at room temperature, and the mixture was stirred at room temperature for 30 min. To this mixture was added a solution of 4-methoxycyclohexanone (3.53 g, 10.0 mmol, prepared according to Shvily, Ronit et al., J. Chem. Soc. Perkin Trans. 2, 1997, 6, 1221) in dimethylsulfoxide (95 mL) dropwise at room temperature, and the mixture was stirred at room temperature for 20 h. Then the mixture was diluted with water (1.0 L), and extracted with diethyl ether (200 mL×6). The combined organic layers were dried over magnesium sulfate, and concentrated in vacuo. The residue was chromatographed on a column of silica gel eluting n-hexane/ethyl acetate (v/v=15/1˜10/1) to give 338 mg (9%, cis) and 204 mg (5%, trans) of the title compound as colorless oil respectively.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07691881B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-ea14e95256c9498cae07544686a60796
Quellennotizuspto-grants-2010_04