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HRID 1292601作成日:2026年10月26日

Pyridine N-Oxide → Methyl 3,3-dimethyl-5-oxovalerate

https://huagongshe.com/reaction/1292601

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Sodium BicarbonateHCID 516892—
反応物Ammonium CarbonateHCID 517111—
反応物Methyl 5-bromo-3,3-dimethylpentanoateHCID 15276782—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Methyl 3,3-dimethyl-5-oxovalerateHCID 301872363%

反応手順

A mixture of methyl 5-bromo-3,3-dimethylpentanoate (5.0 g), pyridine-N-oxide (4.49 g), sodium bicarbonate (3.77 g) and toluene (30 cm3) was heated at the reflux temperature with vigorous agitation for a period of 14 hours. After cooling the mixture to the ambient temperature, water (20 cm3), saturated ammonium carbonate solution (20 cm3) and toluene (50 cm3) were added and the aqueous phase separated and extracted with toluene (3×75 cm3). The toluene extracts were added to the main organic phase and the whole dried over anhydrous magnesium sulphate concentrated by evaporation of the more volatile components under reduced pressure. The residual liquid was purified by Kugelrohr distillation (130° C./water pump pressure) to give methyl 3,3-dimethyl-5-oxopentanoate in 63% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05756835
出典データセットuspto-grants-1998_05
ORD IDord-b85c1265d2ff41958485e1e241bb73ee
出典メモuspto-grants-1998_05