反应详情

3.8 g of dimeric dihydroxyacetone, 25 g of oleic acid, 20 g of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloric acid and 12.9 g of 4-dimethylaminopyridine were added to 150 mL of dichloromethane, and then the solution was stirred for 4 hours at room temperature. The reaction solution was mixed with 0.5 M potassium dihydrogenphosphate solution and subjected to extraction with dichloromethane, and then the extract washed with water and concentrated under reduced pressure after drying. A powder obtained by adding 1 L of methanol to the residue was collected, and then dried. The powder was dissolved in a mixture of 170 mL of tetrahydrofuran and 17 mL of acetic acid solution, and then 1.7 g of sodium borohydride was gradually added. After stirring for 2 hours at room temperature, the reaction solution was mixed with saturated sodium bicarbonate water, and then subjected to extraction with ethyl acetate. The organic layer was concentrated under reduced pressure after drying. The residue was purified with silica gel column chromatography to obtain 14.5 g of the objective compound.

1. extractionsubjected to extraction with dichloromethane
2. washthe extract washed with water
3. concentrationconcentrated under reduced pressure
4. customafter drying
5. customA powder obtained
6. customwas collected
7. customdried
8. dissolutionThe powder was dissolved in a mixture of 170 mL of tetrahydrofuran and 17 mL of acetic acid solution
9. addition1.7 g of sodium borohydride was gradually added
10. stirringAfter stirring for 2 hours at room temperature
11. additionthe reaction solution was mixed with saturated sodium bicarbonate water
12. extractionsubjected to extraction with ethyl acetate
13. concentrationThe organic layer was concentrated under reduced pressure
14. customafter drying
15. customThe residue was purified with silica gel column chromatography