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HRID 31571作成日:2026年10月25日

Sodium hydride → 4-(5,7-Dioxaspiro[2.5]oct-6-ylmethoxy)-2,3-dimethylpyridine 1-oxide

https://huagongshe.com/reaction/31571

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-Chloro-2,3-dimethyl-1-oxidopyridin-1-iumHCID 9877446—
反応物5,7-Dioxaspiro[2.5]oct-6-ylmethanolHCID 59792530—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-(5,7-Dioxaspiro[2.5]oct-6-ylmethoxy)-2,3-dimethylpyridine 1-oxideHCID 5979258857.5%

反応手順

The 5,7-dioxaspiro[2.5]oct-6-ylmethanol (1.7 g, 11.8 mmol) obtained by the step (2b) was mixed with sodium hydride, in oil (708 mg, 17.7 mmol as the content was regarded as 60%) and dimethylsulfoxide (20 ml), and the mixture was stirred at room temperature for 30 minutes. To the reaction mixture, 4-chloro-2,3-dimethylpyridine1-oxide (1.86 g, 11.8 mmol) was added and stirred at 50° C. overnight. After dimethylsulfoxide was distilled off, methanol and NH silica gel were added to the residue and methanol was distilled off. The mixture of the reaction mixture and NH silica gel was purified by silica gel column chromatography (NH silica gel: 200 g, elution solvent: ethyl acetate/heptane=1/1 to 4/1→methanol/ethyl acetate=1/9 to 1/4) to obtain the title compound (1.8 g, yield: 57.5%) as a red oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425634B2
出典データセットuspto-grants-2008_09
ORD IDord-116f90953e3d481eaaea2903b96141af
出典メモuspto-grants-2008_09