Réaction #1747857

Équation de réaction

3,7-dibromo-10-methylphenothiazine

2-naphthylboronic acid

potassium carbonate

→

10-Methyl-3,7-bis(2-naphthyl)phenothiazine

Rendement 82.1%

greenish-yellow solid

Rendement 82.1%

Solvants

dimethoxyethane

water

Conditions de réaction

Traitement

1. 1
   Filtrationfiltered
2. 2
   LavageThe residue was washed with 470 ml of ethanol and hot water
3. 3
   Autredried at 70° C. under reduced pressure
4. 4
   workup.DISSOLUTIONThe solid was dissolved in 200 ml of methylene chloride
5. 5
   Filtrationfiltered through silica gel
6. 6
   AutreAfter the solvent had been removed under reduced pressure

Mode opératoire

9.30 g (25.1 mmol) of 3,7-dibromo-10-methylphenothiazine, 9.50 g (55.2 mmol) of 2-naphthylboronic acid, 0.407 g (0.50 mmol) of bis(triphenylphosphine)palladium dichloride and 3.80 g (27.5 mmol) of potassium carbonate were heated to boiling under reflux under nitrogen for 5 hours in 204 ml of dimethoxyethane and 101 ml of water. The reaction mixture was cooled to room temperature, stirred further overnight and then filtered. The residue was washed with 470 ml of ethanol and hot water, and then dried at 70° C. under reduced pressure. The solid was dissolved in 200 ml of methylene chloride and filtered through silica gel. After the solvent had been removed under reduced pressure, 9.6 g of greenish-yellow solid were obtained (melting point 276-281° C.) and were recrystallized from 500 ml of toluene. 7.10 g (81% of theory) of analytically pure, shiny yellow microcrystals having a melting point of 285-289° C. were obtained, whose solution in chloroform fluoresced at λ=402 nm.

Source