1-methyl-1-(2-methylphenyl)hydrazine

Conditions: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 6.85 g. of 1-methyl-1-(o-toluyl)-hydrazine, 13.8 g. of m-chlorobenzimidic acid ethyl ester and 1.8 g. of the hydrochloride of m-chlorobenzimidic acid ethyl ester is heated with stirring under vacuum for 18 hours and simultaneously ethanol and m-chlorobenzonitrile are distilled off. Then, maintaining the temperature at about 65° C., 40 ml. of ethanol are added followed by a sodium ethylate solution prepared from 0.336 g. of sodium and 20 ml. of ethanol. The mixture is refluxed for 6 hours and after standing over night, the insoluble precipitate is filtered off. The filtrate is evaporated to dryness. The residue is dissolved in 100 ml. of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water, the solution is dried over sodium sulfate. The crude product obtained by evaporation of the diethyl ether solution is crystallized from ethanol. Yield 66%. M.p. 77°-78° C. A mixture of 6.85 g simultaneously ethanol and m-chlorobenzonitrile are distilled off of ethanol are added prepared from 0.336 g The mixture is refluxed for 6 hours after standing over night the insoluble precipitate is filtered off The filtrate is evaporated to dryness The residue is dissolved in 100 ml of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water the solution is dried over sodium sulfate

Conditions: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 6.85 g. of 1-methyl-1-(o-toluyl)-hydrazine, 13.8 g. of m-chlorobenzimidic acid ethyl ester and 1.8 g. of the hydrochloride of m-chlorobenzimidic acid ethyl ester is heated with stirring under vacuum for 18 hours and simultaneously ethanol and m-chlorobenzonitrile are distilled off. Then, maintaining the temperature at about 65° C., 40 ml. of ethanol are added followed by a sodium ethylate solution prepared from 0.336 g. of sodium and 20 ml. of ethanol. The mixture is refluxed for 6 hours and after standing over night, the insoluble precipitate is filtered off. The filtrate is evaporated to dryness. The residue is dissolved in 100 ml. of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water, the solution is dried over sodium sulfate. The crude product obtained by evaporation of the diethyl ether solution is crystallized from ethanol. Yield 66%. M.p. 77°-78° C. A mixture of 6.85 g simultaneously ethanol and m-chlorobenzonitrile are distilled off of ethanol are added prepared from 0.336 g The mixture is refluxed for 6 hours after standing over night the insoluble precipitate is filtered off The filtrate is evaporated to dryness The residue is dissolved in 100 ml of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water the solution is dried over sodium sulfate

Conditions: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 6.85 g. of 1-methyl-1-(o-toluyl)-hydrazine, 13.8 g. of m-chlorobenzimidic acid ethyl ester and 1.8 g. of the hydrochloride of m-chlorobenzimidic acid ethyl ester is heated with stirring under vacuum for 18 hours and simultaneously ethanol and m-chlorobenzonitrile are distilled off. Then, maintaining the temperature at about 65° C., 40 ml. of ethanol are added followed by a sodium ethylate solution prepared from 0.336 g. of sodium and 20 ml. of ethanol. The mixture is refluxed for 6 hours and after standing over night, the insoluble precipitate is filtered off. The filtrate is evaporated to dryness. The residue is dissolved in 100 ml. of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water, the solution is dried over sodium sulfate. The crude product obtained by evaporation of the diethyl ether solution is crystallized from ethanol. Yield 66%. M.p. 77°-78° C. A mixture of 6.85 g simultaneously ethanol and m-chlorobenzonitrile are distilled off of ethanol are added prepared from 0.336 g The mixture is refluxed for 6 hours after standing over night the insoluble precipitate is filtered off The filtrate is evaporated to dryness The residue is dissolved in 100 ml of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water the solution is dried over sodium sulfate

Conditions: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: A mixture of 6.85 g. of 1-methyl-1-(o-toluyl)-hydrazine, 13.8 g. of m-chlorobenzimidic acid ethyl ester and 1.8 g. of the hydrochloride of m-chlorobenzimidic acid ethyl ester is heated with stirring under vacuum for 18 hours and simultaneously ethanol and m-chlorobenzonitrile are distilled off. Then, maintaining the temperature at about 65° C, 40 ml. of ethanol are added followed by a sodium ethylate solution prepared from 0.336 g. of sodium and 20 ml. of ethanol. The mixture is refluxed for 6 hours and after standing over night, the insoluble precipitate is filtered off. The filtrate is evaporated to dryness. The residue is dissolved in 100 ml. of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water, the solution is dried over sodium sulfate. The crude product obtained by evaporation of the diethyl ether solution is crystallized from ethanol. Yield 66%. M.p. 77°-78° C. A mixture of 6.85 g simultaneously ethanol and m-chlorobenzonitrile are distilled off of ethanol are added prepared from 0.336 g The mixture is refluxed for 6 hours after standing over night the insoluble precipitate is filtered off The filtrate is evaporated to dryness The residue is dissolved in 100 ml of diethyl ether and after washing the organic layer successively with aqueous 5% Na2CO3, 5% HCl and water the solution is dried over sodium sulfate