反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
A 500 ml RB flask containing a solution of lauroyl chloride (19.03 g., 87 mM) in dry chloroform (200 ml) was cooled to 0° C. on an ice bath. A solution of N,N-diethyl-1,3-propanediamine (15.00 g., 115 mM) in dry chloroform (25 ml) was added dropwise to the cold solution then allowed to warm to room temperature and stirred for 2 hours. The chloroform was removed under reduced pressure and the residue redissolved in an ethanol/water mixture (1:1) and neutralized with sodium bicarbonate, followed by extraction with chloroform (4×50 ml). The combined extracts were dried (MgSO4), concentrated, and the residue distilled under reduced pressure (bp 176° C., 20μ) to give 21.47 g. (79%) of the subject compound as an amber oil.
WORKUP
后处理
- temperatureto warm to room temperature
- customThe chloroform was removed under reduced pressure
- dissolutionthe residue redissolved in an ethanol/water mixture (1:1)
- extractionfollowed by extraction with chloroform (4×50 ml)
- dry with materialThe combined extracts were dried (MgSO4)
- concentrationconcentrated
- distillationthe residue distilled under reduced pressure (bp 176° C., 20μ)
- customto give 21.47 g