Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486267Generated: November 3, 2026

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

https://huagongshe.com/reaction/1486267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(Diphenylmethylene)amino]acetonitrileHCID 612957—
Reactant1,1-Difluoro-2-iodoethaneHCID 3833565—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117858259HCID 11785825958.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422285B2
Source datasetuspto-grants-2016_08
ORD IDord-6b7e6e7b8ac3479d8d37c14f13924138
Source noteuspto-grants-2016_08