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HRID 888748作成日:2026年10月26日

Stearic Acid → Methyl 3-oxoicosanoate

https://huagongshe.com/reaction/888748

反応式

関与物質

役割名称HCID仕込み量
反応物Stearic AcidHCID 5281—
反応物TriethylamineHCID 8471—
反応物2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
反応物Diethyl cyanophosphonateHCID 76257—
溶媒DichloromethaneHCID 6344—
生成物Methyl 3-oxoicosanoateHCID 84502—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08252755B2
出典データセットuspto-grants-2012_08
ORD IDord-02b8d72175974ef1a07f755ec44e8453
出典メモuspto-grants-2012_08