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
- 24 °C
PROCEDURE
实验过程
Heptanes (1.5 L) and calcium carbonate (150 g; 1.50 mol) were added to the distillation residue from step (a) above and benzyl alcohol (236.8 g; 2.19 mol) was added with stirring at 23-25° C. After stirring for 3.5 hours at 23-25° C., GC analysis indicated approximately 20% of unreacted acyl chloride. After additional stirring for 20 hours, approximately 10% of unreacted acyl chloride was estimated to be present by GC. The resultant mixture was filtered, and the filter cake was washed with heptanes (600 mL). Tetrahydrofuran (200 mL) and a 6% aqueous sodium hydrogen carbonate solution (400 mL) were added to the combined filtrates, and the mixture was stirred for 1 hour at room temperature. The aqueous phase (pH approximately 1) was separated and discarded. The organic phase was washed with water (400 mL) and concentrated at 60° C. under vacuum (down to 25 mmHg). GC analysis on the residue (497.7 g; 85% yield), indicated approximately 7% of unreacted acyl chloride. The hydrolysis of unreacted starting material was forced to completion by addition of further heptanes (1.52 L), tetrahydrofuran (150 mL) and 6% aqueous sodium hydrogen carbonate (600 mL). After stirring for 1 hour at room temperature, less than 1% unreacted acyl chloride was estimated to be present by GC. The aqueous phase (pH approximately 8) was separated and discarded. The organic phase was washed with water (200 mL) and concentrated at 65° C. under vacuum (down to 25 mmHg). This resulted in 418.1 g (72%) of crude title compound as a tea coloured residual oil.
WORKUP
后处理
- additionwas added
- stirringAfter stirring for 3.5 hours at 23-25° C.
- stirringAfter additional stirring for 20 hours
- filtrationThe resultant mixture was filtered
- washthe filter cake was washed with heptanes (600 mL)
- additionTetrahydrofuran (200 mL) and a 6% aqueous sodium hydrogen carbonate solution (400 mL) were added to the combined filtrates
- stirringthe mixture was stirred for 1 hour at room temperature
- customThe aqueous phase (pH approximately 1) was separated
- washThe organic phase was washed with water (400 mL)
- concentrationconcentrated at 60° C. under vacuum (down to 25 mmHg)
- customThe hydrolysis
- stirringAfter stirring for 1 hour at room temperature
- customThe aqueous phase (pH approximately 8) was separated
- washThe organic phase was washed with water (200 mL)
- concentrationconcentrated at 65° C. under vacuum (down to 25 mmHg)