Reaktion #80653

Reaktionsgleichung

2,2,4,4-tetramethyl-6-bromothiochroman

Compound 33

2,2,4,4-tetramethyl-6-bromothiochroman

trimethylsilylacetylene

trimethylsilylacetylene

→

title compound

2,2,4,4-Tetramethyl-6,trimethylsilylethynyl-thiochroman

Lösungsmittel

triethylamine

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigedegassed
2. 2
   SonstigeThe reaction mixture was degassed again
3. 3
   Sonstigethe tube was sealed
4. 4
   Temperaturto cool to room temperature
5. 5
   SonstigeThe mixture was then degassed
6. 6
   Temperaturheated in the sealed tube at 100 degrees C
7. 7
   workup.WAITfor 96 h
8. 8
   TemperaturThe mixture was cooled to room temperature
9. 9
   Extraktionextracted with 3×10 ml of ether
10. 10
    Waschenwashed successively with 25 ml of water and 25 ml of saturated sodium chloride solution
11. 11
    Trocknendried (MgSO4)
12. 12
    SonstigeThe solvent was removed in vacuo
13. 13
    Sonstigethe residue purified by flash chromatography (silica; hexanes followed by 3% ethyl acetate in hexanes)

Vorschrift

A solution of 600 mg (2.11 mmol) of 2,2,4,4-tetramethyl-6-bromothiochroman (Compound 33) in 1.5 ml of triethylamine was placed in a heavy-walled tube and degassed and then treated under argon with 1.4 g (14.3 mmol) of trimethylsilylacetylene and a powdered mixture of 75 mg (0.39 mmol) of cuprous iodide and 150 mg (0.21 mmol) of bis(triphenylphosphine) palladium (II) chloride. The reaction mixture was degassed again, then placed under argon and the tube was sealed. The mixture was heated at 100 degrees C. for 24 h, allowed to cool to room temperature and then treated with a further 1.4 g (14.3 mmol) of trimethylsilylacetylene and a powdered mixture of 75 mg (0.39 mmol) of cuprous iodide and 150 mg (0.21 mmol) of bis(triphenylphosphine) palladium (II) chloride. The mixture was then degassed, placed under argon and then heated in the sealed tube at 100 degrees C. for 96 h. The mixture was cooled to room temperature and extracted with 3×10 ml of ether. The organic extracts were combined, washed successively with 25 ml of water and 25 ml of saturated sodium chloride solution and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by flash chromatography (silica; hexanes followed by 3% ethyl acetate in hexanes) to give the title compound as a yellow, crystalline solid. PMR (CDCl3): & 0.23 (9H, s), 1.36 (6H, s), 1.39 (6H, s), 1.94 (2H, s), 7.17 (1H, dd, J8.2 Hz, 1.8 Hz), 7.25 (1H, d, J-1.8 Hz), 7.30 (1H, d, J-8.2 Hz). MS exact mass, m/1 302.1519 (calcd. for C18H26S Si, 382.1524).

Quelle