10-Hydroxy-2-decanone

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A solution of 95.4 g (370 mmol) of ethyl 9-oxodecanoate ethylene ketal (prepared in Example 22A-1) in 120 ml of ether was added dropwise to a stirred mixture of 10.5 g (277 mmol) of lithium aluminum hydride and 500 ml of ether under argon. The mixture was stirred for 18 hr and then quenched by the dropwise addition of 18 ml of ethyl acetate. To this mixture there was then sequentially added in dropwise fashion, with stirring, 10.5 ml of water, 10.5 ml of 15% aqueous sodium hydroxide and 31.1 ml of water. The mixture was stirred for about 2 to 3 hr and the mixture was then filtered. The filter pad was rinsed several times with ether. The combined filtrates were evaporated in vacuo. The residue was dissolved in a mixture of 250 ml of 10% hydrochloric acid and 120 ml of methanol and left to stand at room temperature for about 4 hr. The solution was evaporated in vacuo. This residue was dissolved in ether and the resulting solution was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo to yield 74.3 g of a yellow oil. The product had the following physical characteristics: quenched by the dropwise addition of 18 ml of ethyl acetate To this mixture there was then sequentially added in dropwise fashion with stirring The mixture was stirred for about 2 to 3 hr the mixture was then filtered The filter pad was rinsed several times with ether The combined filtrates were evaporated in vacuo The residue was dissolved in a mixture of 250 ml of 10% hydrochloric acid and 120 ml of methanol left to stand at room temperature for about 4 hr The solution was evaporated in vacuo This residue was dissolved in ether the resulting solution was washed with saturated aqueous sodium chloride dried over anhydrous magnesium sulfate evaporated in vacuo

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A solution of 95.4 g (370 mmol) of ethyl 9-oxodecanoate ethylene ketal (prepared in Example 22A-1) in 120 ml of ether was added dropwise to a stirred mixture of 10.5 g (277 mmol) of lithium aluminum hydride and 500 ml of ether under argon. The mixture was stirred for 18 hr and then quenched by the dropwise addition of 18 ml of ethyl acetate. To this mixture there was then sequentially added in dropwise fashion, with stirring, 10.5 ml of water, 10.5 ml of 15% aqueous sodium hydroxide and 31.1 ml of water. The mixture was stirred for about 2 to 3 hr and the mixture was then filtered. The filter pad was rinsed several times with ether. The combined filtrates were evaporated in vacuo. The residue was dissolved in a mixture of 250 ml of 10% hydrochloric acid and 120 ml of methanol and left to stand at room temperature for about 4 hr. The solution was evaporated in vacuo. This residue was dissolved in ether and the resulting solution was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo to yield 74.3 g of a yellow oil. The product had the following physical characteristics: quenched by the dropwise addition of 18 ml of ethyl acetate To this mixture there was then sequentially added in dropwise fashion with stirring The mixture was stirred for about 2 to 3 hr the mixture was then filtered The filter pad was rinsed several times with ether The combined filtrates were evaporated in vacuo The residue was dissolved in a mixture of 250 ml of 10% hydrochloric acid and 120 ml of methanol left to stand at room temperature for about 4 hr The solution was evaporated in vacuo This residue was dissolved in ether the resulting solution was washed with saturated aqueous sodium chloride dried over anhydrous magnesium sulfate evaporated in vacuo

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: A solution of 95.4 g (370 mmol) of ethyl 9-oxodecanoate ethylene ketal (prepared in Example 22A-1) in 120 ml of ether was added dropwise to a stirred mixture of 10.5 g (277 mmol) of lithium aluminum hydride and 500 ml of ether under argon. The mixture was stirred for 18 hr and then quenched by the dropwise addition of 18 ml of ethyl acetate. To this mixture there was then sequentially added in dropwise fashion, with stirring, 10.5 ml of water, 10.5 ml of 15% aqueous sodium hydroxide and 31.1 ml of water. The mixture was stirred for about 2 to 3 hr and the mixture was then filtered. The filter pad was rinsed several times with ether. The combined filtrates were evaporated in vacuo. The residue was dissolved in a mixture of 250 ml of 10% hydrochloric acid and 120 ml of methanol and left to stand at room temperature for about 4 hr. The solution was evaporated in vacuo. This residue was dissolved in ether and the resulting solution was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo to yield 74.3 g of a yellow oil. The product had the following physical characteristics: quenched by the dropwise addition of 18 ml of ethyl acetate To this mixture there was then sequentially added in dropwise fashion with stirring The mixture was stirred for about 2 to 3 hr the mixture was then filtered The filter pad was rinsed several times with ether The combined filtrates were evaporated in vacuo The residue was dissolved in a mixture of 250 ml of 10% hydrochloric acid and 120 ml of methanol left to stand at room temperature for about 4 hr The solution was evaporated in vacuo This residue was dissolved in ether the resulting solution was washed with saturated aqueous sodium chloride dried over anhydrous magnesium sulfate evaporated in vacuo