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HRID 231002作成日:2026年10月25日

Pyridine N-Oxide → Ethyl 5-oxopentanoate

https://huagongshe.com/reaction/231002

反応式

関与物質

役割名称HCID仕込み量
反応物Pyridine N-OxideHCID 12753—
反応物Ethyl 5-bromovalerateHCID 84580—
反応物Sodium BicarbonateHCID 516892—
溶媒TolueneHCID 1140—
生成物Ethyl 5-oxopentanoateHCID 1113727948.7%

反応手順

Ethyl 5-bromopentanoate (42 g), sodium bicarbonate (34 g) and pyridine N-oxide (38 g) in toluene (250 ml) are heated together under reflux in an atmosphere of nitrogen with vigorous stirring for 9 hours. After cooling, the product is partitioned with water (400 ml). The toluene layer is separated and the aqueous layer is extracted with a further amount of toluene (100 ml). The combined toluene extracts are dried over magnesium sulphate and the toluene removed by fractional distillation. The residue is distilled under vacuum to give ethyl 5-oxopentanoate as a colourless oil (14.1 g), m.s. M+ 144.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04844892
出典データセットuspto-grants-1989_07
ORD IDord-a6783c418acf471d9a51e7869037a386
出典メモuspto-grants-1989_07