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HRID 736850作成日:2026年10月26日

Water → 2-Methoxy-3,5-heptanedione

https://huagongshe.com/reaction/736850

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl Ethyl KetoneHCID 6569—
反応物Propanoic acid, 2-methoxy-, methyl esterHCID 86599—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Acetic AcidHCID 176—
生成物2-Methoxy-3,5-heptanedioneHCID 2498713162%

反応条件

温度10 °C

反応手順

In a 200 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel was placed 25.0 g (223 mmol) of potassium t-butoxide, and the flask was purged with argon. Then, 100 mL of methylcyclohexanone was placed in the flask. Subsequently, 12.5 g (106 mmol) of methyl 2-methoxypropionate (prepared by the method of Reference Example 1) was dropped under cooling with ice, and further 7.70 g (107 mmol) of 2-butanone was slowly dropped. The mixture was cooled to 10° C. and stirred for 30 minutes for carrying out a reaction. After the reaction was complete, 70 mL of water was placed in the flask under cooling with ice. The aqueous portion was taken out, neutralized with acetic acid, and subjected to extraction with methylcyclohexane. The methylcyclohexane extract was washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated and distilled under reduced pressure (77° C., 1.26 kPa) to give 10.4 g (yield: 62%) of 2-methoxy-3,5-heptanedione 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-1dc7f19806e74dc8875e4596a52c86c4
出典メモuspto-grants-2009_09