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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1259047생성일: 2026년 10월 26일

Ethyl Acetate → 1,3-Diolein

https://huagongshe.com/reaction/1259047

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Oleic AcidHCID 445639—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Dihydroxyacetone dimerHCID 4180364—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물1,3-DioleinHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466255B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-77cfd525dc5047258d2e003676c05383
출처 메모uspto-grants-2013_06