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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888748생성일: 2026년 10월 26일

Stearic Acid → Methyl 3-oxoicosanoate

https://huagongshe.com/reaction/888748

반응식

참여 물질

역할이름HCID투입량
반응물Stearic AcidHCID 5281—
반응물TriethylamineHCID 8471—
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물Diethyl cyanophosphonateHCID 76257—
용매DichloromethaneHCID 6344—
생성물Methyl 3-oxoicosanoateHCID 84502—

반응 단계

Stearic acid (5.0 g, 17.6 mmoles) is suspended in methylene chloride (88 mL) and 2,2-dimethyl-1,3-dioxane-4,6-dione (2.7 g, 18.5 mmoles), triethylamine (6.7 mL, 48.0 mmoles) and diethyl cyanophosphonate (2.7 mL, 17.6 mmoles) are added. All solids dissolve quickly. The solution is stirred for 16 hours at ambient temperature. The reaction mixture is then diluted with methylene chloride (100 mL) and carefully washed three times with aqueous hydrochloric acid (3 M, 50 mL each), three times with water (50 mL each) and once with saturated aqueous sodium chloride (50 mL). The reaction mixture is then dried over anhydrous sodium sulfate, filtered and evaporated. The resulting syrup is dissolved in anhydrous methanol (100 mL) and heated to reflux for 16 hours. The methanol is evaporated and the crude product dissolved in hexanes with slight heating. The crude product was then loaded on silica gel (150 mL bed volume) eluting with hexanes (500 mL) then hexane:acetone (98:2 [v/v], 1000 mL). Fractions containing pure product by thin layer chromatography are pooled and evaporated to dryness. The resulting oil is dried well in vacuo. The yield is 5.2 g (87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252755B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-02b8d72175974ef1a07f755ec44e8453
출처 메모uspto-grants-2012_08