反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
To a 25° C. solution of 1.0 g. (3.32 mmoles) of 3-[4-(1,1-dimethyl-heptyl)-2-hydroxyphenyl]-1,2,5,6-tetrahydropyridine in 15 ml. of acetonitrile is added 1.32 ml. (17.6 mmoles) of 37% formaldehyde solution. After stirring for one hour the reaction is cooled to 0° C. and 332 mg. (5.3 mmole) of sodium cyanoborohydride added. The reaction mixture is allowed to warm to 25° C. over a one hour period while the pH is maintained at 7 by the addition of acetic acid. The reaction mixture is evaporated, made basic with 2 N potassium hydroxyide and extracted with 200 ml. of dichloromethane. The organic extract is dried over magnesium sulfate and evaporated. The residue is crystallized from ether-pentane to yield 350 mg. of the title compound.
WORKUP
后处理
- customTo a 25° C.
- temperatureto warm to 25° C. over a one hour period while the pH
- customThe reaction mixture is evaporated
- extractionextracted with 200 ml
- extractionThe organic extract
- dry with materialis dried over magnesium sulfate
- customevaporated
- customThe residue is crystallized from ether-pentane
- customto yield 350 mg