Réaction #45339

Équation de réaction

H2O

t-butyl nitrite

[3-amino-5-(trifluoromethyl)phenyl]methanol

dimethyl disulfide

→

[3-(methylthio)-5-(trifluoromethyl)phenyl]-methanol

Solvants

CHCl3

Conditions de réaction

Traitement

1. 1
   ExtractionThe mixture was extracted with EtOAc (50 mL)
2. 2
   Lavagewashed with brine (15 mL)
3. 3
   Séchagedried over Na2SO4
4. 4
   Filtrationfiltered
5. 5
   Concentrationconcentrated
6. 6
   AutrePurification by flash chromatography with 0% to 50% EtOAc/hexanes

Mode opératoire

To a solution of [3-amino-5-(trifluoromethyl)phenyl]methanol (319 mg, 1.67 mmol) (Step A, Example 24) in CHCl3 (5 mL) was added dimethyl disulfide (296 μL, 3.34 mmol). Next, t-butyl nitrite (285 μL, 2.4 mmol) was added dropwise by syringe. The reaction was stirred at room temperature for two hours and then poured into H2O (15 mL). The mixture was extracted with EtOAc (50 mL), washed with brine (15 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 0% to 50% EtOAc/hexanes afforded [3-(methylthio)-5-(trifluoromethyl)phenyl]-methanol. The [3-(methylthio)-5-(trifluoromethyl)phenyl]methanol was contaminated with minor impurities that were removed after the next step. Rf=0.53 (50% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.63 (s, 1H), 7.40 (s, 1H), 7.35 (s, 1H), 4.71 (s, 2H), 2.51 (s, 3H).

Source