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HRID 1809363Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1809363

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
PatentnummerUS08362038B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-c7b290177d6340a1b494980bf6f5a1b5
Quellennotizuspto-grants-2013_01