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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1616716생성일: 2026년 10월 26일

Dihydroferulic Acid → 8-Methylnonyl 3-(4-hydroxy-3-methoxyphenyl)propionate

https://huagongshe.com/reaction/1616716

반응식

참여 물질

역할이름HCID투입량
반응물Dihydroferulic AcidHCID 14340—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물IsodecanolHCID 32898—
용매TolueneHCID 1140—
생성물8-Methylnonyl 3-(4-hydroxy-3-methoxyphenyl)propionateHCID 6898598076.5%

반응 조건

온도50 °C

반응 단계

8-Methyl-1-nonanol (752 mg, 4.74 mmol), 3-(4-hydroxy-3-methoxyphenyl)propionic acid (977 mg, 4.98 mmol) and Novozyme 435 (100 mg) were measured and placed in a flask (25 ml). Toluene (5 ml) and anhydrous magnesium sulfate (1 g) were added, and the mixture was stirred with heating in an oil bath at 50° C. for 16 hr. The reaction mixture was allowed to cool to room temperature, toluene (25 ml) was added, and Novozyme 435 and the precipitated insoluble material were removed by filtration. Toluene (50 ml) was added, and the mixture was washed with 5% aqueous sodium hydrogen carbonate solution (25 ml×3) and saturated brine (25 ml) and dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was developed by PTLC (chloroform:n-hexane:ethyl acetate=1:1:1), and silica gel containing the object product was stirred with ethyl acetate (100 ml) for 30 min for extraction. The silica gel was filtered off, and the filtrate was concentrated under reduced pressure to give 8-methylnonyl 3-(4-hydroxy-3-methoxyphenyl)propionate (1.22 g, yield 76.2%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765809B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-50e64329e11f49d6a8ea37592a1fa5f7
출처 메모uspto-grants-2014_07