참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Oleic Acid | HCID 445639 | — |
| 반응물 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 반응물 | Dihydroxyacetone dimer | HCID 4180364 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 1,3-Diolein | HCID 5497165 | — |
반응 단계
3.8 g of dihydroxyacetone dimer, 25 g of oleic acid, g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt, and 12.9 g of 4-dimethylaminopyridine were dissolved in 150 mL of dichloromethane, for reaction under agitation at ambient temperature for 4 hours. The organic layer was washed by adding aqueous 0.5 M potassium dihydrogen phosphate solution to the reaction solution. After the organic layer was dried and concentrated under reduced pressure, 1 L of methanol was added to the resulting residue; the generated powder was filtered and recovered, and then dried. The dried powder was dissolved in a mixture solution of 170 mL of tetrahydrofuran and 17 mL of aqueous 10% acetic acid solution, to which 1.7 g of sodium borohydride was added in small portions at 0° C. Subsequently, the resulting mixture was agitated at ambient temperature for 2 hours to promote the reaction. The resulting reaction solution was poured in saturated aqueous sodium hydrogen carbonate, for extraction with ethyl acetate. After the organic layer was dried, the organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography, to obtain 14.5 g of the intended product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08466255B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-77cfd525dc5047258d2e003676c05383 |
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| 출처 메모 | uspto-grants-2013_06 |
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