1,4-二(2-乙基己氧基)-1,4-二氧丁烷-2-磺酸

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

实验步骤: In a reaction vessel charged with a magnetic stirbar and protected from light, 5.0 g (29 mmol) of silver nitrate was dissolved in approximately 100 mL of deionized water. To the stirred solution was added, is small portions, 13.1 g (29 mmol) of sodium docusate. As the docusate was added, the solution became gradually gelatinous with attendant difficulties in stirring that were remedied by gently heating the solution. After addition of the final portion of sodium docusate, the warmed solution/suspension was stirred overnight, after which point it was rotary evaporated to yield a slightly tan mass. The mass was extracted with a chloroform-acetonitrile mixture, into which much of the material dissolved but some white solid (presumed to be NaNO3) did not. The mixture was filtered and evaporated under reduced pressure to give a soft mass of slightly off-white final product (which should be stored away from light because it is photosensitive). This material was soluble in lidocaine docusate, some organic solvents, and was relatively slow to dissolve in water, doing so to only a limited degree. The two ions have known antimicrobial and emollient properties, respectively. In a reaction vessel charged with a magnetic stirbar To the stirred solution was added by gently heating the solution the warmed solution/suspension was stirred overnight after which point it was rotary evaporated to yield a slightly tan mass The mass was extracted with a chloroform-acetonitrile mixture, into which much of the material dissolved The mixture was filtered evaporated under reduced pressure

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

实验步骤: In a reaction vessel charged with a magnetic stirbar and protected from light, 5.0 g (29 mmol) of silver nitrate was dissolved in approximately 100 mL of deionized water. To the stirred solution was added, is small portions, 13.1 g (29 mmol) of sodium docusate. As the docusate was added, the solution became gradually gelatinous with attendant difficulties in stirring that were remedied by gently heating the solution. After addition of the final portion of sodium docusate, the warmed solution/suspension was stirred overnight, after which point it was rotary evaporated to yield a slightly tan mass. The mass was extracted with a chloroform-acetonitrile mixture, into which much of the material dissolved but some white solid (presumed to be NaNO3) did not. The mixture was filtered and evaporated under reduced pressure to give a soft mass of slightly off-white final product (which should be stored away from light because it is photosensitive). This material was soluble in lidocaine docusate, some organic solvents, and was relatively slow to dissolve in water, doing so to only a limited degree. The two ions have known antimicrobial and emollient properties, respectively. In a reaction vessel charged with a magnetic stirbar To the stirred solution was added by gently heating the solution the warmed solution/suspension was stirred overnight after which point it was rotary evaporated to yield a slightly tan mass The mass was extracted with a chloroform-acetonitrile mixture, into which much of the material dissolved The mixture was filtered evaporated under reduced pressure