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
50.0 g (0.13 mol) of the compound of Example 4 in 500 ml. of methanol and 1 ml of acetic acid was hydrogenated in a rocking autoclave at room temperature and 200 psi in the presence of 6 g. of Raney nickel. After the hydrogen uptake (3 equivalents) was complete the filtered reaction mixture was concentrated in vacuo to a volume of 140 ml. Toluene (600 ml.) was added and the remaining methanol was removed by azeotropic distillation. The mixture was heated at reflux for an additional 30 minutes and then allowed to cool to room temperature. The precipitate was collected, washed with toluene and dried to yield 42.3 g (97%) of white crystals, m.p. 179-180° (lit. m.p. 179°). The analytical sample was prepared by recrystallization from ethaniol: m.p. 180-181°.
WORKUP
后处理
- customwas hydrogenated in a rocking autoclave at room temperature
- customthe filtered reaction mixture
- concentrationwas concentrated in vacuo to a volume of 140 ml
- additionToluene (600 ml.) was added
- customthe remaining methanol was removed by azeotropic distillation
- temperatureThe mixture was heated
- temperatureat reflux for an additional 30 minutes
- customThe precipitate was collected
- washwashed with toluene
- customdried