Reacción #595389

Ecuación de reacción

KOH

3,6-dibromocarbazole

Epibromohydrin

→

desired product

Rendimiento 66.3%

3,6-Dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole

Rendimiento 66.3%

Disolventes

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.DISSOLUTIONuntil dissolved
2. 2
   workup.STIRRINGthe reaction was stirred at room temperature overnight
3. 3
   OtroUpon completion, the solution was partitioned between EtOAc and H2O
4. 4
   LavadoThe aqueous layer was washed 3× with EtOAc
5. 5
   Lavadothe combined organics were washed with saturated aqueous NaCl
6. 6
   Secadodried over Na2SO4
7. 7
   Filtraciónfiltered
8. 8
   Concentraciónconcentrated in vacuo
9. 9
   OtroThe crude residue was recrystallized from EtOAc/Hexane

Procedimiento

Following a literature procedure (Asso, V.; Ghilardi, E.; Bertini, S.; Digiacomo, M.; Granchi, C.; Minutolo, F.; Rapposelli, S.; Bortolato, A.; Moro, S. Macchia, M. ChemMedChem, 2008, 3, 1530-1534) powdered KOH (0.103 g, 1.85 mmol) was added to a solution of 3,6-dibromocarbazole (0.500 g, 1.54 mmol) in DMF (1.5 mL) at ambient temperature and stirred for 30 min until dissolved. Epibromohydrin (0.32 mL, 3.8 mmol) was added via syringe and the reaction was stirred at room temperature overnight. Upon completion, the solution was partitioned between EtOAc and H2O. The aqueous layer was washed 3× with EtOAc, and the combined organics were washed with saturated aqueous NaCl, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was recrystallized from EtOAc/Hexane to afford the desired product (389 mg, 66%).

Fuente