Réaction #6653

Équation de réaction

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

Solvants

isopropanol

Conditions de réaction

Traitement

1. 1
   Autrethe isopropanol was removed under vacuum
2. 2
   ExtractionThe residue was extracted with ether
3. 3
   Extractionthe ether extract
4. 4
   Lavagewas washed successively with water and saturated NaCl solution
5. 5
   Séchagedried (MgSO4)
6. 6
   AutreThe solvent was removed vacuo
7. 7
   Autrethe residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes)

Mode opératoire

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).

Source