Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetonitrile → 4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro- | HCID 16057 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 4-(Biphenyl-2-yloxy)-3,5,6-trichlorophthalonitrile | HCID 117902707 | — |
반응 단계
To a 250 mL flask, 4.8 g of tetrachlorophthalonitrile, 4.3 g of biphenyl-2-ol, 5 g of potassium carbonate (K2CO3) and 55 mL of acetonitrile are added, followed by heating for 12 hours while refluxing. After completion of the reaction, 30 mL of ethyl acetate is added and filtered to remove the solvent. To the obtained solid, a suitable amount of dichloromethane is added to dissolve the solid, followed by adding hexane for crystallization. The obtained solid is filtered and dried under vacuum to obtain a compound, 4-[(biphenyl-2-yl)oxy]-3,5,6-trichlorophthalonitrile. The second step reaction may be represented by Reaction Scheme 2:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09341743B2 |
| 출처 데이터셋 | uspto-grants-2016_05 |
| ORD ID | ord-9f221331d5624b8793ac8825c68b4545 |
| 출처 메모 | uspto-grants-2016_05 |