Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenylphosphine → 4-(4-Chlorophenyl)benzonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Benzonitrile, 4-bromo- | HCID 12162 | — |
| 반응물 | HCID 178478983 | HCID 178478983 | — |
| 촉매 | Palladium Chloride | HCID 24290 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(4-Chlorophenyl)benzonitrile | HCID 1394308 | 75% |
반응 단계
4-chlorophenylmagnesium chloride (114 g, 18% solution in tetrahydrofuran) is added dropwise over seven hours to a refluxing solution of 4-bromobenzonitrile (20 g), palladium (II) chloride (0.78 g ) and triphenylphosphine (2.3 g) in tetrahydrofuran (100 ml). [HPLC: yield 75-79%]. After cooling to room temperature tetrahydrofuran is removed under vacuum. The residue is taken up in toluene/water (1:1) (200 ml) and filtered. The aqueous phase is separated off, and the solvent removed by distillation. The crude product is recrystallised from isopropanol/ethanol to give 4'-chlorobiphenyl-4-carbonitrile as a solid, m.pt. 128-130° C. 1H NMR (CDCl3): 2.41(s,3H), 7.46(d,2H), 7.53(d,2H), 7.65(d,2H), 7.74(d,2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06121480 |
| 출처 데이터셋 | uspto-grants-2000_09 |
| ORD ID | ord-d37c410c20a94ee0802651aebd966662 |
| 출처 메모 | uspto-grants-2000_09 |