참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Stearic Acid | HCID 5281 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| 반응물 | Diethyl cyanophosphonate | HCID 76257 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 3-oxoicosanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08252755B2 |
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| 출처 데이터셋 | uspto-grants-2012_08 |
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| ORD ID | ord-02b8d72175974ef1a07f755ec44e8453 |
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| 출처 메모 | uspto-grants-2012_08 |
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