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
PROCEDURE
实验过程
2-(9-Fluorenyl) ethanol was prepared from a solution of fluorene (116.35 g, 0.7 mmol) in 800 ml of dry THF at -20° C. which was added n-Buli in hexane (0.7 mol) keeping the temperature below -10° C. To the clear solution was rapidly added 357 ml of 1.4M ethylene oxide in ether (0.5 mol) keeping the temperature below 5° C. The reaction mixture was stirred for 5 hours, then quenched with 50 ml of saturated ammonium chloride solution. The THF was removed at a rotary evaporator. The residue was partitioned between water and ethyl acetate. The organic layer was separated, dried with MgSO4 and concentrated in vacuo until crystallization began. The solution was allowed to stand overnight and the crystals were collected and dried (mp 97° C.) (85.5 g, (81%)).
WORKUP
后处理
- customthe temperature below -10° C
- customthe temperature below 5° C
- customquenched with 50 ml of saturated ammonium chloride solution
- customThe THF was removed at a rotary evaporator
- customThe residue was partitioned between water and ethyl acetate
- customThe organic layer was separated
- dry with materialdried with MgSO4
- concentrationconcentrated in vacuo until crystallization
- waitto stand overnight
- customthe crystals were collected
- customdried (mp 97° C.) (85.5 g, (81%))