Réaction #1448232

Équation de réaction

2-bromo-hexanoic acid methyl ester

4-fluoro-3-methyl-benzenethiol

triethylamine

→

title compound

Rendement 92.0%

2-(4-Fluoro-3-methyl-phenylsulfanyl)-hexanoic acid methyl ester

Rendement 92.0%

Solvants

dichloromethane

dichloromethane

Conditions de réaction

Traitement

1. 1
   Lavagewashed with 1N HCl and brine
2. 2
   SéchageThe organic layer dried over anhydrous Na2SO4
3. 3
   AutreAfter removing the solvent under reduced pressure
4. 4
   Autrethe product was isolated by Flash chromatography (silica gel)
5. 5
   Lavageeluting with 0-20% ethyl acetate/hexanes

Mode opératoire

To a solution of 2-bromo-hexanoic acid methyl ester (0.500 g, 2.404 mmol) and 4-fluoro-3-methyl-benzenethiol (0.340 g, 2.404 mmol) in 20 mL of dichloromethane, was added triethylamine (3.3 mL, 12.020 mmol). After stirring at room temperature under N2 for 46 h, the reaction mixture was diluted with dichloromethane and washed with 1N HCl and brine. The organic layer dried over anhydrous Na2SO4. After removing the solvent under reduced pressure, the product was isolated by Flash chromatography (silica gel) eluting with 0-20% ethyl acetate/hexanes to give the title compound as colorless oil (0.596 g, 92% yield). LC-MS: tR=11.2 min; m/z 271 (M+H)+.

Source