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HRID 736848作成日:2026年10月26日

Acetone → 5-Methoxyhexane-2,4-dione

https://huagongshe.com/reaction/736848

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Sodium amideHCID 24533—
反応物Propanoic acid, 2-methoxy-, methyl esterHCID 86599—
反応物Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物5-Methoxyhexane-2,4-dioneHCID 2498677953%

反応手順

In a 200 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel was placed 10.1 g (259 mmol) of sodium amide, and the flask was purged with argon. Then, 120 mL of methylcyclohexane was placed in the flask. Subsequently, 7.40 g (127 mmol) of acetone was slowly dropped into the ice-cooled mixture in the flask, and the resulting mixture was stirred for 15 minutes. Into the flask was further dropped 15.0 g (127 mmol) of methyl 2-methoxypropionate (prepared by the method of Reference Example 1), and the mixture was stirred for 30 minutes for carrying out a reaction. After the reaction was complete, 50 mL of water was placed in the flask under cooling with ice. The aqueous portion was taken out, made acetic with acetic acid, and subjected to extraction with hexane. The hexane extract was washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated and distilled under reduced pressure (66° C., 1.38 kPa) to give 9.63 g (yield: 53%) of 2-methoxy-3,5-hexanedione as colorless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07595414B2
出典データセットuspto-grants-2009_09
ORD IDord-d3d528aa383f468a8d67cab1ec6ede37
出典メモuspto-grants-2009_09