[(Diphenylmethylene)amino]acetonitrile → HCID 117858259, compound

Temperature

-78 °C

18 g (81.72 mmol) of [(diphenylmethylene)amino]acetonitrile were initially charged in 500 ml of abs. THF, and 39.22 ml (98.06 mmol) of n-butyllithium (2.5 N in hexane) were added at −78° C. under argon, and the mixture was stirred at −78° C. for a further 15 min. Subsequently, the reaction solution was warmed up to 0° C. 17.25 g (89.89 mmol) of 1,1-difluoro-2-iodoethane were added dropwise to the reaction solution, which was stirred at 0° C. for a further 15 min. The reaction solution was quenched with water at 0° C., ethyl acetate was added and the mixture was washed three times with semisaturated aqueous sodium chloride solution. The combined aqueous phases were reextracted twice with ethyl acetate. The combined organic phases were dried over sodium sulphate, filtered and concentrated by rotary evaporation. The residue was purified by means of silica gel chromatography (eluent:dichloromethane/cyclohexane 1/1). 13.57 g of the target compound were obtained (49% of theory, 84% purity).

1. temperatureSubsequently, the reaction solution was warmed up to 0° C
2. stirringwas stirred at 0° C. for a further 15 min
3. customThe reaction solution was quenched with water at 0° C.
4. additionethyl acetate was added
5. washthe mixture was washed three times with semisaturated aqueous sodium chloride solution
6. dry with materialThe combined organic phases were dried over sodium sulphate
7. filtrationfiltered
8. concentrationconcentrated by rotary evaporation
9. customThe residue was purified by means of silica gel chromatography (eluent:dichloromethane/cyclohexane 1/1)

ORD record

ord-6b7e6e7b8ac3479d8d37c14f13924138

Source dataset

uspto-grants-2016_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09422285B2