反应 #5167

反应方程式

sodium chloride

(2S, 4R)-1-(t-butoxycarbonyl)-4-hydroxy-2-pyrrolidinecarboxylic acid

ethyl chloroformate

methylamine

→

title compound

(2S, 4R)-1-(t-Butoxycarbonyl)-2-methylcarbamoyl-4-hydroxypyrrolidine

溶剂

tetrahydrofuran

triethylamine

tetrahydrofuran

反应条件

后处理

1. 1
   其他to rise to room temperature
2. 2
   workup.WAITto continue for 1 hour
3. 3
   萃取extracted thrice with ethyl acetate
4. 4
   洗涤The combined extracts were washed with an aqueous solution of sodium chloride
5. 5
   干燥dried over anhydrous magnesium sulfate
6. 6
   其他The solvent was then removed by distillation under reduced pressure

实验过程

9.91 ml of triethylamine were added at -40° C. to a solution of 15.03 g of (2S, 4R)-1-(t-butoxycarbonyl)-4-hydroxy-2-pyrrolidinecarboxylic acid dissolved in 250 ml of dry tetrahydrofuran, and then a solution of 6.81 ml of ethyl chloroformate in 30 ml of dry tetrahydrofuran was added at -30° to -40° C. to the resulting mixture, which was then stirred at the same temperature for 1 hour, 16.82 ml of a 40% by volume aqueous methylamine solution were then added at -30° C., and the temperature of the reaction mixture was allowed to rise to room temperature; the reaction was then allowed to continue for 1 hour. At the end of this time, the reaction mixture was mixed with a small amount of an aqueous solution of sodium chloride and extracted thrice with ethyl acetate. The combined extracts were washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, giving 12.76 g of the title compound as a colorless oil.

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