Reaktion #54758

Reaktionsgleichung

2-furylethyl mesylate

4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline

sodium hydride

pentane

→

N-(2-Furylethyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline

Lösungsmittel

dimethylformamide

dimethylformamide

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturheated at 50° under nitrogen
2. 2
   TemperaturThe mixture was heated at 90° for 2 hours
3. 3
   Temperaturcooled to 35°
4. 4
   Temperaturthe reaction mixture heated at 90° overnight
5. 5
   Temperaturcooled
6. 6
   Extraktionextracted with ether
7. 7
   SonstigeEvaporation of the ether
8. 8
   Sonstigegave an oil which
9. 9
   Sonstigewas purified by column chromatography (Silicar CC-7, eluting with acetone-benzene)

Vorschrift

A solution of 5.0 g (18.5 mmoles) of 4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline in 100 ml of anhydrous dimethylformamide was added to a stirred suspension of 1.4 g (28 mmoles) of 50% sodium hydride in mineral oil (washed with pentane) in 75 ml of anhydrous dimethylformamide heated at 50° under nitrogen. The mixture was heated at 90° for 2 hours, then cooled to 35°. A solution of 7.1 g (37 mmoles) of freshly prepared 2-furylethyl mesylate (prepared according ot the procedure of Crossland and Servis, J. Org. Chem., 35, 3195 (1970)) in 10 ml of anhydrous dimethylformamide was added and the reaction mixture heated at 90° overnight. It was the cooled and poured into ice-water, and extracted with ether. Evaporation of the ether gave an oil which was purified by column chromatography (Silicar CC-7, eluting with acetone-benzene). The major fraction was identified as N-(2-furylethyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline

Quelle