Reaktion #80662

Reaktionsgleichung

aluminum chloride

2,2,4,4,7-pentamethyl-chroman

Compound 46

2,2,4,4,7-pentamethyl-chroman

HCl

acetyl chloride

→

title compound

2,2,4,4,7-Pentamethyl-6-acetyl-chroman

Lösungsmittel

ether

water

nitromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturcooled in an ice-bath
2. 2
   Sonstigewas waned to room temperature
3. 3
   SonstigeThe organic layer was separated
4. 4
   Extraktionthe aqueous layer extracted with ether
5. 5
   Waschenwashed successively with water, saturated NaHCO3 solution, water again
6. 6
   Trocknensaturated NaCl solution, and then dried (MgSO4)
7. 7
   SonstigeThe solvent was removed in vacuo
8. 8
   Sonstigethe residue was purified by flash chromatography (silica; 5% ethyl acetate in hexanes)

Vorschrift

To an ice-bath cooled solution of 1.96 g (9.6 mmol) of 2,2,4,4,7-pentamethyl-chroman (Compound 46) in 30 ml of nitromethane was added under argon 1.059 g (13.5 mmol) of acetyl chloride followed by 1.9 g (14.3 mmol) of aluminum chloride. The reaction mixture was stirred at room temperature for 14 h and then cooled in an ice-bath and treated with 25 ml of conc. HCl. The mixture was waned to room temperature and diluted with ether and water. The organic layer was separated and the aqueous layer extracted with ether. The organic extracts were combined and washed successively with water, saturated NaHCO3 solution, water again, and saturated NaCl solution, and then dried (MgSO4). The solvent was removed in vacuo and the residue was purified by flash chromatography (silica; 5% ethyl acetate in hexanes) to give the title compound as a pale yellow oil. PMR (CDCl3): & 1.36 (6H, s), 1.37 (6H, s), 1.86 (2H, s), 2.49 (3H, s), 2.56 (3H, s), 6.65 (1H, s), 7.74 (1H, s).

Quelle