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
PROCEDURE
实验过程
To a solution of the 2-carbomethoxy-3-tropanone obtained in example 4 (17 g, 85 mmol) in 750 ml methanol cooled to -35° C. was added sodium borohydride (17 g, 450 mmol) and the mixture was stirred for 4 hours. The cooled solution was quenched by slow addition of concentrated hydrochloric acid (40 ml) and the mixture was concentrated in vacuo. Water (400 ml) was added and the pH was adjusted to 3 by addition of concentrated hydrochloric acid. After having washed the water phase three times with diethyl ether pH was adjusted to 11 by addition of concentrated ammonium hydroxide and the water phase was extracted three times with methylene chloride. Concentration in vacuo yielded oil which was dissolved in ethanol and added concentrated hydrochloric acid followed by concentration in vacuo. Freeze drying of the residue yielded the title compound as an amorphous product.
WORKUP
后处理
- customThe cooled solution was quenched by slow addition of concentrated hydrochloric acid (40 ml)
- concentrationthe mixture was concentrated in vacuo
- additionWater (400 ml) was added
- additionthe pH was adjusted to 3 by addition of concentrated hydrochloric acid
- washAfter having washed the water phase three times with diethyl ether
- additionpH was adjusted to 11 by addition of concentrated ammonium hydroxide
- extractionthe water phase was extracted three times with methylene chloride
- concentrationConcentration in vacuo
- customyielded oil which
- concentrationfollowed by concentration in vacuo
- customFreeze drying of the residue