Organic Syntheses, Coll. Vol. 3, p.597 (1955); Vol. 22, p.94 (1942).
In a 1-l. Claisen flask
is placed a mixture of 64 g. of finely divided sodium amide (Note 1)
and 100 g. of acetyl-o-toluidine (Note 2)
. About 50 ml. of dry ether
is added (Note 3)
, and the apparatus is swept out with dry nitrogen
. Then, with a slow current of nitrogen
passing through the mixture, the reaction flask (Note 4)
is heated in a metal bath (Note 5)
. The temperature is raised to 240–260° over a 30-minute period and is maintained in this range for 10 minutes. A vigorous evolution of gas occurs, the cessation of which indicates that the reaction is complete (Note 6)
. The metal bath is removed, the flask is allowed to cool, and 50 ml. of 95% ethanol
and 250 ml. of warm (about 50°) water are added, successively, to the reaction mixture. The decomposition of the sodium derivative of 2-methylindole
, and of any excess sodium amide
, is completed by warming the mixture gently with a Bunsen burner
. The cooled reaction mixture is extracted with two 200-ml. portions of ether (Note 7)
. The combined ether
extracts are filtered, and the filtrate is concentrated to about 125 ml. The solution is then transferred to a 250-ml. modified Claisen flask
and distilled. The 2-methylindole
distils at 119–126° /3–4 mm. as a water-white liquid, which rapidly solidifies in the receiver to a white crystalline mass. This product melts at 56–57°
. The yield is 70–72 g.
) (Note 8)
The product may be further purified by dissolving it in 100 ml. of methanol
, adding 30 ml. of water, and allowing the solution to stand in the ice chest for 5 hours. The pure white plates (52 g.) melt at 59°. An additional 10 g. may be recovered by cooling the filtrate after it has been diluted with about 20 ml. of water.
The sodium amide
was ground in an open mortar
, and at no time was difficulty experienced. As a precautionary measure, the grinding could be carried out under ether
Acetyl-o-toluidine, m.p. 110–111°, obtained from the Eastman Kodak Company
, was used. After the reactants are introduced into the flask, they should be mixed thoroughly with a long spatula
is added to facilitate the formation of the sodium
salt of the amide.
It is advisable to cover the bottom of the reaction flask with soot, to prevent the metal from adhering to the glass.
Sand and salt baths are not satisfactory.
Reaction begins when the bath temperature has risen to approximately 200°. Frothing occurs, and the froth solidifies. The checkers found it necessary to stir the solidified froth into the reaction mixture, so that heating of the whole mass could be uniform. This stirring is necessary throughout—i.e., from the beginning of vigorous gas evolution until completion of the period of heating.
may be isolated, less conveniently, by steam distillation; the crystalline product (m.p. about 56–57°) can be filtered from the cold distillate.
The method described here is of general application to substituted acetyl- and benzoyl-o-toluidines
The cyclization of acetyl-o-toluidine
has been reported to occur in low yield on distillation with zinc
Better yields have been obtained by heating the toluidide
with sodium ethoxide
or with barium oxide
in a current of hydrogen
A vapor-phase cyclization over a silica-alumina
catalyst has also been reported.5
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