참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Cyanide | HCID 8929 | — |
| 반응물 | 1-Chloro-4-(trifluoromethoxy)benzene | HCID 2777273 | — |
| 촉매 | Triphenylphosphine | HCID 11776 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | Methyl Ethyl Ketone | HCID 6569 | — |
| 생성물 | 4-(Trifluoromethoxy)benzonitrile | HCID 67621 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06162942 |
|---|
| 출처 데이터셋 | uspto-grants-2000_12 |
|---|
| ORD ID | ord-e599be7ad45e47fa97d053716ad39bf6 |
|---|
| 출처 메모 | uspto-grants-2000_12 |
|---|