Reaction #2139932
ord-7d2196d0a09441f3bd870125976e9caa
Reaction equation
Solvents
Conditions
Workup
- 1Temperaturewas refluxed for 24 hours
- 2TemperatureAfter cooling
- 3Filtrationthe reaction mixture was filtered
- 4Otherthe solvent was evaporated
- 5OtherThe product was crystallized from methanol
- 6Otherwas 103-104° C
Procedure
A mixture of 10 g (0.05 mol) of phenothiazine (obtained from Fluka), 11.7 g (0.075 mol) of iodoethane (obtained from Aldrich), 4.2 g (0.075 mol) of potassium hydroxide, and 0.25 g of tetra-n-butylammonium hydrogen sulfate (obtained from Aldrich) in 200 ml of dry toluene was refluxed for 24 hours. After cooling, the reaction mixture was filtered, and the solvent was evaporated. The product was crystallized from methanol. The yield of 10-ethylphenothiazine was 10.2 g (90%). The melting point of the product was 103-104° C. The 1H-NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (δ, ppm): 1.40 (t, J=7.0 Hz, 3H, CH3); 3.90 (q, J=7.0 Hz, 2H, CH2); 6.78-7.32 (m, 8H, Ar).