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HRID 1809363作成日:2026年10月27日

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

https://huagongshe.com/reaction/1809363

反応式

関与物質

役割名称HCID仕込み量
反応物CycloateHCID 14337—
反応物Sodium hydrideHCID 24758—
反応物Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
反応物4-MethoxycyclohexanoneHCID 535028—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物6-Methoxy-1-oxaspiro[2,5]octaneHCID 15329490—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362038B2
出典データセットuspto-grants-2013_01
ORD IDord-c7b290177d6340a1b494980bf6f5a1b5
出典メモuspto-grants-2013_01