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
- 120 °C
PROCEDURE
实验过程
To a sealable vial was added ethyl 4-((1R,3 aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-amino-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)cyclohex-3-enecarboxylate (0.2 g, 0.356 mmol), 1-bromo-2-chloroethane (0.295 mL, 3.56 mmol) and phosphoric acid, potassium salt (0.378 g, 1.780 mmol). The mixture was diluted with acetonitrile (5 mL), was flushed with nitrogen, then sealed and heated to 120° C. After 24 h of heating, the mixture was cooled to rt. The reaction mixture was filtered to remove solids, then the solids were washed with dichloromethane and the filtrate was concentrated under reduced pressure to give the title compound (0.21 g, 0.357 mmol, 100% yield) as an off-white solid. LCMS: m/e 588.7 (M+H)+, 2.21 min (method 5).
WORKUP
后处理
- customwas flushed with nitrogen
- customsealed
- temperatureAfter 24 h of heating
- temperaturethe mixture was cooled to rt
- filtrationThe reaction mixture was filtered
- customto remove solids
- washthe solids were washed with dichloromethane
- concentrationthe filtrate was concentrated under reduced pressure