Reaktion #82878

Reaktionsgleichung

triethylamine

2-Naphthol

naphthol

morpholine

chlorine

→

1-chloro-4-morpholino-2-naphthol

Ausbeute 109.5%

Lösungsmittel

toluene

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturby warming
2. 2
   TemperaturThe pale brown solution was cooled
3. 3
   Sonstigeto precipitate
4. 4
   Sonstigeat 15°-20° C
5. 5
   FiltrationThe resulting brown mixture was filtered
6. 6
   Sonstigeto remove triethylamine hydrochloride as a white amorphous solid
7. 7
   WaschenThe toluene filtrate was washed with water
8. 8
   Sonstigedried
9. 9
   Sonstigeevaporated

Vorschrift

2-Naphthol (28.8 g; 0.200 mol) was dissolved in toluene (200 ml) by warming. The pale brown solution was cooled and vigorously stirred until the naphthol began to precipitate and chlorine (31.29 g;0.442 mol) was then passed through the solution at approximately 2.5-3.0 g/min followed immediately by nitrogen gas. The resulting amber solution was treated firstly with triethylamine (24.68 g;0.244 mol) in one portion and then with a solution of morpholine (17.40 g;0.20 mol) in toluene (180 ml) dropwise over 1.5 hours keeping the temperature at 15°-20° C. The resulting brown mixture was filtered to remove triethylamine hydrochloride as a white amorphous solid. The toluene filtrate was washed with water, dried and evaporated to give 1-chloro-4-morpholino-2-naphthol as a brown viscous oil (57.76 g). Purification by chromatography over silica (eluent: 15% ethyl acetate in toluene) gave the product as an off-white solid (34.37 g;65%). Further purification by crystallisation from toluene gave the product as a white solid, m.pt. 163°-65° C. ##STR18## (b) 4-Morpholino-2-naphthol

Quelle