反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 48 °C
PROCEDURE
实验过程
Compound 96A (7.58 g) was dissolved in THF (120 mL). To this solution was added 5% aq. HCl (100 mL). The reaction mixture was heated at 48° C. for 90 min. After cooling to room temperature, the reaction mixture was quenched with sat. NaHCO3 solution until no more CO2 was released. The solution was concentrated under vacuum. The residue was re-dissolved in EtOAc, and treated with water (500 mL). The organic layer was separated, and the aqueous layer was extracted with additional EtOAc (three times). The combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated under vacuum. The residue was purified with flash column chromatography on silica gel eluting with 7:3/Hex:EtOAc to give 5.5 g of the title compound 96B (78%): APCI (+)LC/MS: 543 (M+H)+.
WORKUP
后处理
- temperatureAfter cooling to room temperature
- customthe reaction mixture was quenched with sat. NaHCO3 solution until no more CO2
- concentrationThe solution was concentrated under vacuum
- dissolutionThe residue was re-dissolved in EtOAc
- additiontreated with water (500 mL)
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with additional EtOAc (three times)
- washThe combined organic layers were washed with brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated under vacuum
- customThe residue was purified with flash column chromatography on silica gel eluting with 7:3/Hex