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HRID 2412342Erstellt: 25. Oktober 2026

3,5-Dimethylaniline → 2-[(5,7-Dimethylbenzothiazol-2-ylimino)methylene]propanedinitrile

https://huagongshe.com/reaction/2412342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-DimethylanilineHCID 7949—
EduktAmmonium thiocyanateHCID 15666—
EduktBromineHCID 24408—
Edukt2-(Ethoxymethylene)propanedinitrileHCID 67152—
Edukt(3,5-Dimethylphenyl)thioureaHCID 736215—
Edukt5,7-Dimethyl-1,3-benzothiazol-2-amineHCID 2049896—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
Produkt5,7-Dimethyl-1,3-benzothiazol-2-amineHCID 2049896—
Produkt2-[(5,7-Dimethylbenzothiazol-2-ylimino)methylene]propanedinitrileHCID 2043306072,7%

Reaktionsschritte

2-Amino-5,7-dimethylbenzothiazole was prepared by treatment of 3,5-dimethylaniline with ammonium thiocyanate and conversion of the resulting N-(3,5-dimethylphenyl)thiourea with bromine and chloroform (Barnikow and Bodeker Ber. 100(5), 1394), m.p. 142°-144°. 2-Amino-5,7-dimethylbenzothiazole, 6.16 g. (34.5 millimoles) was added to a solution of a pea-sized piece of sodium in 40 ml. of anhydrous ethanol. Ethoxymethylenemalononitrile, 4.22 g. (34.5 millimoles), was added to the solution and the mixture was heated at reflux for about 2 hrs. The precipitated solid was collected by filtration, washed with ethanol, and dried in vacuo at 100°, yielding 6.93 g. (72.7%) of the desired product which was a yellow solid, m.p. 239°-241°. A small portion was recrystallized from 95% ethanol and submitted for analysis, m.p. 241°-243°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04491587
Quelldatensatzuspto-grants-1985_01
ORD IDord-af1fd4ce1aa147b7be794f955a196df1
Quellennotizuspto-grants-1985_01