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HRID 736850생성일: 2026년 10월 26일

Water → 2-Methoxy-3,5-heptanedione

https://huagongshe.com/reaction/736850

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl Ethyl KetoneHCID 6569—
반응물Propanoic acid, 2-methoxy-, methyl esterHCID 86599—
반응물Potassium tert-butoxideHCID 23665647—
용매Acetic AcidHCID 176—
생성물2-Methoxy-3,5-heptanedioneHCID 2498713162%

반응 조건

온도10 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595414B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-1dc7f19806e74dc8875e4596a52c86c4
출처 메모uspto-grants-2009_09