Реакция #2379360
ord-ee0bba5fdbb14f93b9745041b11137bb
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1Концентрированиеconcentrated in vacuo
- 2Промывкаwashed with diisopropylether
- 3workup.DISSOLUTIONThe oil was dissolved in a mixture of water (15 ml) and sodium bicarbonate
- 4workup.ADDITIONwas added until the pH of the solution
- 5workup.ADDITIONThe mixture of water (6 ml) and acetone (20 ml)
- 6workup.ADDITIONwas added to the solution and palmitoyl chloride (2.20 g)
- 7workup.ADDITIONwas added in one portion
- 8workup.STIRRINGAfter stirring for 30 minutes at room temperature
- 9Концентрированиеthe reaction mixture was concentrated
- 10workup.ADDITIONTo the residue was added water (30 ml)
- 11Другоеthe precipitates was collected
- 12Другоеdried
- 13Другоеto give a crude product, which
- 14Другоеwas purified by column chromatography of Silicagel (90 g) with chloroform-methanol (30:1
Методика
Trifluoroacetic acid (15 ml) was added to Boc-L-Ala-D-Glu-(OH)OBzl (1)(3.26 g) and the mixture was stirred for 20 minutes at room temperature, concentrated in vacuo and washed with diisopropylether. The oil was dissolved in a mixture of water (15 ml) and sodium bicarbonate was added until the pH of the solution became 8-9. The mixture of water (6 ml) and acetone (20 ml) was added to the solution and palmitoyl chloride (2.20 g) was added in one portion. After stirring for 30 minutes at room temperature, the pH of the solution was adjusted to 3 with 1N-hydrochloric acid and the reaction mixture was concentrated. To the residue was added water (30 ml) and the precipitates was collected and dried to give a crude product, which was purified by column chromatography of Silicagel (90 g) with chloroform-methanol (30:1, v/v) as an eluent to give palmitoyl-L-Ala-D-Glu(OH)OBzl (2)(2.00 g). mp. 131°-132° C.