돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1954485생성일: 2026년 10월 26일

Triphenylphosphine → 4-(4-Chlorophenyl)benzonitrile

https://huagongshe.com/reaction/1954485

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Benzonitrile, 4-bromo-HCID 12162—
반응물HCID 178478983HCID 178478983—
촉매Palladium ChlorideHCID 24290—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Chlorophenyl)benzonitrileHCID 139430875%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06121480
출처 데이터셋uspto-grants-2000_09
ORD IDord-d37c410c20a94ee0802651aebd966662
출처 메모uspto-grants-2000_09