Reaktion #81560

Reaktionsgleichung

1,1-dimethyl-5-nitro-3-phenyl-1H-indene

→

crude title compound

Ausbeute 98.7%

5-Amino-1,1-dimethyl-3-phenyl-1H-indene

Ausbeute 98.7%

Lösungsmittel

benzene

water

water

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturat reflux
2. 2
   workup.STIRRINGThe resulting mixture was stirred
3. 3
   Temperaturat reflux for additional 18 hours
4. 4
   Filtrationfiltered through a pad of celite
5. 5
   ExtraktionThe filtrate was extracted with ethyl acetate (20 mL×3)
6. 6
   TrocknenThe combined extracts were dried over magnesium sulfate

Vorschrift

To a mixture of 1,1-dimethyl-5-nitro-3-phenyl-1H-indene (0.56 g, 2.11 mmol) in 5 mL of benzene was added 33% ferric chloride (1 mL) and 4 mL of water. The mixture was stirred at reflux and iron powder 1.00 g, 5.28 mmol) was added in four portions during 2 hours. The resulting mixture was stirred at reflux for additional 18 hours. The mixture was diluted with 20 mL of water and 20 mL of ethyl acetate, and filtered through a pad of celite. The filtrate was extracted with ethyl acetate (20 mL×3). The combined extracts were dried over magnesium sulfate to give 0.49 g (98% yield) of the crude title compound which was not further purified and used in the next reaction; 1H-NMR (CDCl3) δ1.37 (s, 6H), 6.40 (s, 1H), 6.71 (dd, J=2.0, 7.9 Hz, 1H), 6.93 (d, J=2.0 Hz, 1H), 7.19 (d, J=7.9 Hz, 1H), 7.36-7.58 (m, 5H); MS m/e 236 (MH+).

Quelle