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
- -78 °C
PROCEDURE
实验过程
n-Butyllithium (34 ml of a 2.5M solution in hexanes) was added to a solution of 1-bromo-3-ethylbenzene (15 g) in tetrahydrofuran (320 ml) at −78° C. After 1 hour N,N-dimethylformamide (15 ml) was added. The mixture was stirred at −78° C. for 1 hour and allowed to warm to room temperature. The mixture was quenched with aqueous ammonium chloride and partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated. The residue was dissolved in methanol (250 ml) and treated with sodium borohydride (1.51 g) portionwise. The mixture was stirred at room temperature for 16 hours, quenched with 2M HCl (100 ml) and stirred for 4 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ethyl acetate and 2M HCl. The organic phase was dried (MgSO4), evaporated and the residue purified by chromatography eluting with 5-10% ethyl acetate in isohexane.
WORKUP
后处理
- temperatureto warm to room temperature
- customThe mixture was quenched with aqueous ammonium chloride
- custompartitioned between ethyl acetate and water
- dry with materialThe organic phase was dried (MgSO4)
- customevaporated
- dissolutionThe residue was dissolved in methanol (250 ml)
- additiontreated with sodium borohydride (1.51 g) portionwise
- stirringThe mixture was stirred at room temperature for 16 hours
- customquenched with 2M HCl (100 ml)
- stirringstirred for 4 hours
- concentrationThe mixture was concentrated under reduced pressure
- customthe residue partitioned between ethyl acetate and 2M HCl
- dry with materialThe organic phase was dried (MgSO4)
- customevaporated
- customthe residue purified by chromatography
- washeluting with 5-10% ethyl acetate in isohexane