3-diethoxyphosphorylpropanal

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154°-155° C. NMR (CDCl3): δ1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154°-155° C. NMR (CDCl3): δ1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154-155° C. NMR (CDCl3): δ 1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154-155° C. NMR (CDCl3): δ 1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154°-155° C. NMR (CDCl3): δ1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154-155° C. NMR (CDCl3): δ 1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure

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

Procedure: A solution of 1-trityl-1,2,4-triazole (10.0 g, prepared as described in Example 1) and N,N,N',N'-tetramethylethylenediamine (3.8 g) in dry tetrahydrofuran (250 ml) was cooled to -70° C. under nitrogen. n-Butyllithium (22.2 ml, 1.6M solution in hexane) was added dropwise, with stirring, at such a rate that the internal temperature was maintained below -60° C. The red solution was stirred at -70° C. for twenty-five minutes, then treated dropwise with diethyl 3-oxo-propane phosphonate (6.20 g, prepared by formic acid deacetalisation of the diethyl acetal, DE 2517448, and also described in, for example, Tetrahedron 1981, 37, 1377) whilst maintaining the temperature at that level. The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution. It was extracted with ethyl acetate and the organic phase washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure to give crude diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-5-yl)propane phosphonate (10.81 g). Chromatography on silica, using dichloromethane-ethanol (19:1) as eluant, gave pure material, m.p. 154°-155° C. NMR (CDCl3): δ1.3(6H,t), 1.9(2H,m), 1.7(2H,m), 3.1(1H,br), 4.0(4H,m), 4.1(1H,t), 7.1-7.3 (15H,m), 7.9(1H,s). M/S: M+ 505. at such a rate that the internal temperature was maintained below -60° C The red solution was stirred at -70° C. for twenty-five minutes whilst maintaining the temperature at that level The mixture was stirred for two and a half hours at -70° C. then quenched, at that temperature, with saturated aqueous ammonium chloride solution It was extracted with ethyl acetate the organic phase washed with brine dried over magnesium sulphate evaporated under reduced pressure