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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1259048생성일: 2026년 10월 26일

Methanol → Glyceryl 1,3-distearate

https://huagongshe.com/reaction/1259048

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Stearic AcidHCID 5281—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Dihydroxyacetone dimerHCID 4180364—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
생성물Glyceryl 1,3-distearateHCID 10126933.6%

반응 단계

3.0 g of dihydroxyacetone dimer, 22.7 g of stearic acid, 16.8 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt, and 10.8 g of 4-dimethylaminopyridine were dissolved in 100 mL of dichloromethane, for overnight reaction under agitation at ambient temperature. Adding 0.5 L of methanol to the reaction solution, the generated powder was filtered and recovered. The powder recovered by filtration was washed with methanol. After the washed powder was dried, 6 g of the dried powder was dissolved in a mixture solution of 400 mL of tetrahydrofuran and 20 mL of aqueous 10% acetic acid solution, to which 1.1 g of sodium borohydride was added in small portions at 0° C. Subsequently, the resulting mixture was agitated at ambient temperature for 6 hours to promote the reaction. The resulting reaction solution was poured in saturated aqueous sodium hydrogen carbonate, for extraction in 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 3.5 g of the intended product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466255B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-71d110c218a04a70bb1fd932f2cf64bd
출처 메모uspto-grants-2013_06