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HRID 1809363생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1809363

반응식

참여 물질

역할이름HCID투입량
반응물CycloateHCID 14337—
반응물Sodium hydrideHCID 24758—
반응물Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
반응물4-MethoxycyclohexanoneHCID 535028—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물6-Methoxy-1-oxaspiro[2,5]octaneHCID 15329490—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362038B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-c7b290177d6340a1b494980bf6f5a1b5
출처 메모uspto-grants-2013_01