反应详情
EQUATION
反应方程式
REACTANTS
反应物
Sodium cyanide (Na(CN))
CNNa
2-Bromo-1-(3,4-difluorophenyl)ethan-1-one
C8H5BrF2O
3-(4-isopropylphenyl)-3-oxopropanenitrile
C12H13NO
3-(2,5-Difluorophenyl)-3-oxopropanenitrile
C9H5F2NO
3-(2,4-Dichlorophenyl)-3-oxopropanenitrile
C9H5Cl2NO
未命名化合物
3-(3,4-Dimethylphenyl)-3-oxopropanenitrile
C11H11NO
未命名化合物
未命名化合物
未命名化合物
3-Oxo-3-{4-[(propan-2-yl)oxy]phenyl}propanenitrile
C12H13NO2
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of 13.2 g. (0.056 mole) of 3,4-difluorophenacyl bromide was dissolved in 100 ml. of ethanol and cooled to 5° C. in ice. A solution of 7.6 g. (0.16 mole) of sodium cyanide in 40 ml. of water was added dropwise over 0.5 hr. and the reaction is stirred for an additional one hour. At that time, the mixture was diluted with 100 ml. of water and filtered through Celite®. Acidification of the filtrate gave a cloudy mixture which was extracted with methylene chloride. The organic phase was dried, filtered through Magnesol® and evaporated. Recrystallization of the residue from carbon tetrachloride provides 5.3 g. (52%) of colorless solid, m.p. 74°-75° C. Similarly prepared were 2,4-dichlorobenzoylacetonitrile, o-ethylbenzoylacetonitrile, p-isopropylbenzoylacetonitrile, m-isobutylbenzoylacetonitrile, 3,4-dimethylbenzoylacetonitrile, m-ethoxybenzoylacetonitrile, p-isopropoxybenzoylacetonitrile, 3,4-diethoxybenzoylacetonitrile, and 2,5-difluorobenzoylacetonitrile.
WORKUP
后处理
- additionAt that time, the mixture was diluted with 100 ml
- filtrationof water and filtered through Celite®
- customAcidification of the filtrate gave a cloudy mixture which
- extractionwas extracted with methylene chloride
- customThe organic phase was dried
- filtrationfiltered through Magnesol®
- customevaporated
- customRecrystallization of the residue from carbon tetrachloride
- customprovides 5.3 g
- customSimilarly prepared