Reaktion #602327

Reaktionsgleichung

sodium hydroxide

2-ethylsulfanyl-6-methyl-4-morpholin-4-yl-benzamide

4-chlorobenzyl bromide

→

N-[(4-chlorophenyl)-methyl]-2-ethylsulfanyl-6-methyl-4-morpholin-4-yl-benzamide

Ausbeute 50.0%

Lösungsmittel

benzene tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter completion of the reaction (monitored by TLC)
2. 2
   Sonstigethe organic layer is separated
3. 3
   Extraktionthe aqueous layer is extracted with ethyl acetate (2×20 ml)
4. 4
   WaschenThe organic layer is washed with water (20 ml), brine (20 ml)
5. 5
   Trocknendried over anhydrous sodium sulfate
6. 6
   Sonstigeevaporated
7. 7
   Sonstigeto get the crude product, which
8. 8
   Sonstigeis purified by column chromatography (silica gel, 28% ethyl acetate/hexane)

Vorschrift

To a solution of 2-ethylsulfanyl-6-methyl-4-morpholin-4-yl-benzamide (synthesized according to the methods described in sections b) and c) of example 1) (0.20 g, 0.71 mmol) in benzene-tetrahydrofuran (1:1) (16 ml) are added tetrabutylammonium hydrogensulfate (0.024 g, 0.071 mmol) and 50% sodium hydroxide solution (6 ml) at RT. The reaction mixture is heated to 70° C. and 4-chlorobenzyl bromide (0.15 g, 0.71 mmol) is added. The reaction mixture is stirred at 70° C. for 20 min. After completion of the reaction (monitored by TLC), the organic layer is separated and the aqueous layer is extracted with ethyl acetate (2×20 ml). The organic layer is washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 28% ethyl acetate/hexane) to yield N-[(4-chlorophenyl)-methyl]-2-ethylsulfanyl-6-methyl-4-morpholin-4-yl-benzamide (example 2) (0.095 g, 0.24 mmol, 50%). [M+H]+ 405.1.

Quelle