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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2088667생성일: 2026년 10월 25일

Acetonitrile → 3-Amino-3-(2,4-dichlorophenyl)acrylonitrile

https://huagongshe.com/reaction/2088667

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물DiisopropylamineHCID 7912—
반응물n-Butyl lithiumHCID 61028—
반응물2,4-DichlorobenzonitrileHCID 81050—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-Amino-3-(2,4-dichlorophenyl)acrylonitrileHCID 66911322—

반응 단계

Under argon, 90 g (889.46 mmol) of diisopropylamine were initially charged in 1660 ml of THF at −70° C. in a three-necked flask with mechanical stirrer. 124.66 ml of N-butyllithium solution (2.5 M in hexane, 758.66 mmol) were added dropwise at such a rate that the temperature did not exceed −60° C. The mixture was stirred for 10 min, and a solution of 32.22 g (784.82 mmol) of acetonitrile in 340 ml of THF was then slowly added dropwise and the suspension was stirred for 30 min. A solution of 90 g (523.21 mmol) of 2,4-dichlorobenzonitrile in 340 ml of THF was then added dropwise, and the mixture was stirred at −70° C. for 20 min. The mixture was allowed to slowly warm to RT and stirred at RT for a further 16 h. 600 ml of water were added, most of the THF was distilled off and water and dichloromethane were added. The organic phase was washed with saturated aqueous sodium chloride solution. Removal of the solvent gave crystals which were purified by trituration with diethyl ether. This gave 76.5 g (69% of theory) of the product as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436003B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-cebb1e0ed83a4ba4b6d18e0e701c5e20
출처 메모uspto-grants-2013_05