돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1275925생성일: 2026년 10월 25일

Sodium Cyanide → 4-(Trifluoromethoxy)benzonitrile

https://huagongshe.com/reaction/1275925

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanideHCID 8929—
반응물1-Chloro-4-(trifluoromethoxy)benzeneHCID 2777273—
촉매TriphenylphosphineHCID 11776—
촉매ZincHCID 23994—
용매Methyl Ethyl KetoneHCID 6569—
생성물4-(Trifluoromethoxy)benzonitrileHCID 6762166%

반응 단계

Under an atmosphere of nitrogen, a mixture of 6.5 g of bis-triphenylphosphine-nickel dichloride, 5 g of triphenylphosphine and 120 ml of MEK was stirred at room temperature for 10 minutes. 1.9 g of activated zinc powder were then added, and the reaction mixture was stirred at 70° C. for 30 minutes. Following this, the mixture was allowed to cool to 25° C., and 93.25 g of 1-chloro-4-trifluoromethoxybenzene were added dropwise. The mixture was stirred for 10 minutes, 24 g of sodium cyanide were added, and the reaction mixture was stirred at from 65 to 70° C. for 20 h. The conversion was then approximately 75% (GC). After cooling to room temperature, the mixture was filtered, the solid filter residue was washed 2× with 50 ml of MEK and the combined organic phases were concentrated under reduced pressure. Vacuum distillation gave 58.5 g (66% of theory) of 4-trifluoromethoxybenzonitrile as a colourless liquid (boiling point at 120 mbar: 80° C.). 2.6% of coupling products had formed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06162942
출처 데이터셋uspto-grants-2000_12
ORD IDord-e599be7ad45e47fa97d053716ad39bf6
출처 메모uspto-grants-2000_12