Reacción #1960509
ord-4929171ffb444b968d69b2b4be69e024
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroto obtain the clear solution
- 2OtroAt the end of 40 min.
- 3workup.ADDITIONthe mixture was poured
- 4ExtracciónThe residue was extracted into ethyl acetate (100 ml×2)
- 5Lavadowashed with water (100 ml×2) and ethyl acetate layer
- 6Secadowas dried over anhydrous sodium sulfate
- 7FiltraciónAfter filtration, ethyl acetate
- 8Otrowas removed
- 9Otrothe residue was dried
Procedimiento
A mixture containing 4-Fluorophenylhydrazine hydrochloride (5.0 g; 30.75 mmol; ALDRICH), 3-methyl-2-butanone (3.7 g; 43 mmol; ALDRICH) and acetic acid (30 ml) was stirred for 30 min. under nitrogen to obtain the clear solution. The mixture was then refluxed at 130° C. The appearance of UV-Vis Abs. Max at 255 nm and the disappearance of the peak at 282 nm confirmed the formation of the indole. At the end of 40 min. the reaction was stopped and the mixture was poured into crushed ice (100 g). The residue was extracted into ethyl acetate (100 ml×2), washed with water (100 ml×2) and ethyl acetate layer was dried over anhydrous sodium sulfate. After filtration, ethyl acetate was removed, and the residue was dried to give 4.15 g of the indole (Yield 76%).