ethyl 2-methylnonanoate

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of diisopropylamine (10.7 ml, 76.6 mmol) in anhydrous THF (100 ml) was added dropwise n-butyl lithium (1.61N, 47.6 ml, 76.6 mmol) at -78° C. under argon stream. After stirring the mixture at -78° C. for 30 minutes, ethyl 2-methylnonanoate (9.6028 g, 47.9 mmol) was added dropwise and the mixture was further stirred at -78° C. for 30 minutes. A solution of methyl iodide (5.5 ml, 88.3 mmol) in HMPA (2.5 ml, 14.4 mmol) was dropwise added and the mixture was stirred at -78° C. for 40 minutes, them at 0° C. for 40 minutes, and further at room temperature for 45 minutes. Saturated aqueous ammonium chloride solution (20 ml) was added and the reaction mixture was extracted with ethyl acetate (50 ml×4). The ethyl acetate layers were washed with water (50 ml) and with brine (50 ml), dried over anhydrous sodium sulfate, and concentrated. Distillation gave ethyl 2,2-dimethylnonanoate (9.6627 g, 94.1% yield, b.p.: 53°-65.5° C./0.22 mmHg) as colorless liquid. The structure of this product was confirmed by the following data. the mixture was further stirred at -78° C. for 30 minutes the mixture was stirred at -78° C. for 40 minutes them at 0° C. for 40 minutes further at room temperature for 45 minutes the reaction mixture was extracted with ethyl acetate (50 ml×4) The ethyl acetate layers were washed with water (50 ml) and with brine (50 ml) dried over anhydrous sodium sulfate concentrated Distillation

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of diisopropylamine (9.0 ml, 64.4 mmol) in 100 ml anhydrous THF was added dropwise n-butyl lithium (1.61N, 40.0 ml, 64.4 mmol) at -78° C. under argon atmosphere. The mixture was stirred at -78° C. for 30 minutes and ethyl nonanoate (10.00 g, 53.7 mmol) was added dropwise. After stirring the mixture at -78° C. for 30 minutes, a solution of methyl iodide (3.7 ml, 59.1 mmol) in HMPA (2.8 ml, 16.1 mmol) was added dropwise and the mixture was stirred at -78° C. for 3.5 hours. Saturated aqueous solution of ammonium chloride (20 ml) was added to the reaction mixture and the resulting mixture was then extracted with ether (50 ml×4). The ether layers were washed with water (50 ml) and with brine (50 ml), dried over anhydrous sodium sulfate, and concentrated. Distillation gave yellow liquid, ethyl 2-methylnonanoate (9.6892 g, yield: 90.1%, b.p.: 63°-64° C./0.7 mmHg). The structure of this product was confirmed by the following data. After stirring the mixture at -78° C. for 30 minutes the mixture was stirred at -78° C. for 3.5 hours the resulting mixture was then extracted with ether (50 ml×4) The ether layers were washed with water (50 ml) and with brine (50 ml) dried over anhydrous sodium sulfate concentrated Distillation

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of diisopropylamine (9.0 ml, 64.4 mmol) in 100 ml anhydrous THF was added dropwise n-butyl lithium (1.61N, 40.0 ml, 64.4 mmol) at -78° C. under argon atmosphere. The mixture was stirred at -78° C. for 30 minutes and ethyl nonanoate (10.00 g, 53.7 mmol) was added dropwise. After stirring the mixture at -78° C. for 30 minutes, a solution of methyl iodide (3.7 ml, 59.1 mmol) in HMPA (2.8 ml, 16.1 mmol) was added dropwise and the mixture was stirred at -78° C. for 3.5 hours. Saturated aqueous solution of ammonium chloride (20 ml) was added to the reaction mixture and the resulting mixture was then extracted with ether (50 ml×4). The ether layers were washed with water (50 ml) and with brine (50 ml), dried over anhydrous sodium sulfate, and concentrated. Distillation gave yellow liquid, ethyl 2-methylnonanoate (9.6892 g, yield: 90.1%, b.p.: 63°-64° C./0.7 mmHg). The structure of this product was confirmed by the following data. After stirring the mixture at -78° C. for 30 minutes the mixture was stirred at -78° C. for 3.5 hours the resulting mixture was then extracted with ether (50 ml×4) The ether layers were washed with water (50 ml) and with brine (50 ml) dried over anhydrous sodium sulfate concentrated Distillation

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of diisopropylamine (10.7 ml, 76.6 mmol) in anhydrous THF (100 ml) was added dropwise n-butyl lithium (1.61N, 47.6 ml, 76.6 mmol) at -78° C. under argon stream. After stirring the mixture at -78° C. for 30 minutes, ethyl 2-methylnonanoate (9.6028 g, 47.9 mmol) was added dropwise and the mixture was further stirred at -78° C. for 30 minutes. A solution of methyl iodide (5.5 ml, 88.3 mmol) in HMPA (2.5 ml, 14.4 mmol) was dropwise added and the mixture was stirred at -78° C. for 40 minutes, them at 0° C. for 40 minutes, and further at room temperature for 45 minutes. Saturated aqueous ammonium chloride solution (20 ml) was added and the reaction mixture was extracted with ethyl acetate (50 ml×4). The ethyl acetate layers were washed with water (50 ml) and with brine (50 ml), dried over anhydrous sodium sulfate, and concentrated. Distillation gave ethyl 2,2-dimethylnonanoate (9.6627 g, 94.1% yield, b.p.: 53°-65.5° C./0.22 mmHg) as colorless liquid. The structure of this product was confirmed by the following data. the mixture was further stirred at -78° C. for 30 minutes the mixture was stirred at -78° C. for 40 minutes them at 0° C. for 40 minutes further at room temperature for 45 minutes the reaction mixture was extracted with ethyl acetate (50 ml×4) The ethyl acetate layers were washed with water (50 ml) and with brine (50 ml) dried over anhydrous sodium sulfate concentrated Distillation

Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: To a solution of diisopropylamine (9.0 ml, 64.4 mmol) in 100 ml anhydrous THF was added dropwise n-butyl lithium (1.61N, 40.0 ml, 64.4 mmol) at -78° C. under argon atmosphere. The mixture was stirred at -78° C. for 30 minutes and ethyl nonanoate (10.00 g, 53.7 mmol) was added dropwise. After stirring the mixture at -78° C. for 30 minutes, a solution of methyl iodide (3.7 ml, 59.1 mmol) in HMPA (2.8 ml, 16.1 mmol) was added dropwise and the mixture was stirred at -78° C. for 3.5 hours. Saturated aqueous solution of ammonium chloride (20 ml) was added to the reaction mixture and the resulting mixture was then extracted with ether (50 ml×4). The ether layers were washed with water (50 ml) and with brine (50 ml), dried over anhydrous sodium sulfate, and concentrated. Distillation gave yellow liquid, ethyl 2-methylnonanoate (9.6892 g, yield: 90.1%, b.p.: 63°-64° C./0.7 mmHg). The structure of this product was confirmed by the following data. After stirring the mixture at -78° C. for 30 minutes the mixture was stirred at -78° C. for 3.5 hours the resulting mixture was then extracted with ether (50 ml×4) The ether layers were washed with water (50 ml) and with brine (50 ml) dried over anhydrous sodium sulfate concentrated Distillation