Reacción #6653

Ecuación de reacción

4,4-dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinoline

Compound 95

4,4-dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinoline

KOH

→

title compound

4,4-Dimethyl-6-ethynyl-1,2,3,4-tetrahydroquinoline

Disolventes

isopropanol

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrothe isopropanol was removed under vacuum
2. 2
   ExtracciónThe residue was extracted with ether
3. 3
   Extracciónthe ether extract
4. 4
   Lavadowas washed successively with water and saturated NaCl solution
5. 5
   Secadodried (MgSO4)
6. 6
   OtroThe solvent was removed vacuo
7. 7
   Otrothe residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes)

Procedimiento

To a solution of 569 mg (2.21 mmol) of 4,4-dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinoline (Compound 95) in 3 ml of isopropanol was added, under argon, 1 ml of 1N aqueous KOH solution. The reaction mixture was stirred at room temperature for 36 h and the isopropanol was removed under vacuum. The residue was extracted with ether and the ether extract was washed successively with water and saturated NaCl solution and then dried (MgSO4). The solvent was removed vacuo and the residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a brown oil. PMR (CDCl3): δ 1.26 (6H, s), 1.65-1.72 (2H, m), 2.96 (1H, s), 3.27-3.34 (2H, m), 6.34 (1H, d, J~8.3 Hz), 7.08 (1H, dd, J~8.3 Hz, 1.6 Hz), 7.33 (1H, d, J~1.6 Hz).

Fuente