反应 #7937

反应方程式

EtSH

AlCl3

HCl

NaHCO3

9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)-ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one

→

9a-butyl-7-hydroxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one

溶剂

EtOAc

water

tetrahydrofuran

CH2Cl2

反应条件

后处理

1. 1
   其他contained in an ice-cold flask
2. 2
   workup.WAITat room temperature for 35 minutes
3. 3
   温度The mixture was cooled in an ice bath
4. 4
   workup.STIRRINGstirred at 0° C. for 10 minutes
5. 5
   workup.STIRRINGstirred
6. 6
   其他The layers were separated
7. 7
   萃取the aqueous portion extracted with EtOAc
8. 8
   洗涤The combined organics were washed with brine
9. 9
   干燥dried over MgSO4
10. 10
    过滤filtered
11. 11
    其他evaporated under vacuum

实验过程

An ice-cold solution of 9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)-ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one (85 mg, 96% weight pure, 0.172 mmol) in anhydrous CH2Cl2 (1.2 mL) was placed under a nitrogen atmosphere and treated with EtSH (0.055 mL, 0.743 mmol). The resulting solution was added by syringe to AlCl3 (115.2 mg, 0.864 mmol) contained in an ice-cold flask and kept under nitrogen. The resulting solution was stirred at 0° C. for 3 minutes, then at room temperature for 35 minutes. The mixture was cooled in an ice bath, treated with 0.5N HCl (1.6 mL) and tetrahydrofuran (1.0 mL), and stirred at 0° C. for 10 minutes. The resulting mixture was diluted with EtOAc (20 mL) and water (15 mL) and stirred while basifying with solid NaHCO3. The layers were separated and the aqueous portion extracted with EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered, and evaporated under vacuum to afford 9a-butyl-7-hydroxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one as a yellow semi-solid.

来源