2-ethyl-1,3-diphenylpropane-1,3-dione

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80° C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice-water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling to give 6.47 g (56%) of product, m.p. 80° C to 81° C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80°C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80°C to 81°C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80°C to 81°C.

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80°C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80°C to 81°C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80°C to 81°C.

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80° C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice-water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling to give 6.47 g (56%) of product, m.p. 80° C to 81° C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80° C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice-water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling to give 6.47 g (56%) of product, m.p. 80° C to 81° C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80°C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80° to 81°C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80° to 81°C.

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80°C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80°C to 81°C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil which is crystallized from hexane with cooling to give 6.47 g (56%) or product, m.p. 80°C to 81°C.

Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Methylhydrazine (2.86 g, 0.06 mole) is added to an isopropanol (100 ml) solution of 1,3-diphenyl-2-ethyl-1,3-propanedione (11.0 g, 0.044 mole) with constant stirring at 80° C. The reaction mixture is heated at reflux for 31/2 hours, then stirred at room temperature overnight. The reaction mixture is poured into ice-water, stirred for 1/2 hour, and the resulting mixture extracted with chloroform (3×50 ml). Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling to give 6.47 g (56%) of product, m.p. 80° C to 81° C. The reaction mixture is heated at reflux for 31/2 hours stirred at room temperature overnight stirred for 1/2 hour the resulting mixture extracted with chloroform (3×50 ml) Evaporation of the organic layer gives an oil, which is crystallized from hexane with cooling