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 3.43 g. (10.15 mmol) of the end product of Example 15 in 60 ml. of absolute EtOH, was added 12 ml. of hydrazine-hydrate. The reaction was heated to reflux for 17 hours, then cooled and concentrated in vacuo. The residue was taken up in 60 ml. toluene; 1.0 g. potassium t-butoxide added and the mixture heated to reflux for 8 hours, then cooled to room temperature and stirred for 9 hours. The reaction was poured over ice and brine and toluene added. The toluene phase was separated and dried over Na2SO4. The aqueous phase was extracted well with CH2Cl2 and the combined extracts dried over Na2SO4. The dried solutions were combined and concentrated and the crude product recrystallized from THF/hexane to give the desired end product, mp 258°-261°. An analytical sample was prepared by an additional recrystallization from THF/hexane and was obtained as colorless crystals: mp 259°-261°.
WORKUP
后处理
- temperatureThe reaction was heated
- temperatureto reflux for 17 hours
- temperaturecooled
- concentrationconcentrated in vacuo
- additionpotassium t-butoxide added
- temperaturethe mixture heated
- temperatureto reflux for 8 hours
- additionThe reaction was poured over ice and brine and toluene
- additionadded
- customThe toluene phase was separated
- dry with materialdried over Na2SO4
- extractionThe aqueous phase was extracted well with CH2Cl2
- dry with materialthe combined extracts dried over Na2SO4
- concentrationconcentrated
- customthe crude product recrystallized from THF/hexane
- customto give the desired end product, mp 258°-261°
- customwas obtained as colorless crystals