돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 617200생성일: 2026년 10월 25일

Triphenylphosphine → [1,1'-Biphenyl]-4-amine, 3-nitro-

https://huagongshe.com/reaction/617200

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-Bromo-2-nitroanilineHCID 70132—
반응물TributylphenyltinHCID 607632—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매DimethylformamideHCID 6228—
생성물[1,1'-Biphenyl]-4-amine, 3-nitro-HCID 7770575.2%

반응 단계

A solution of 4-bromo-2-nitroaniline 17 (1.0 g, 4.67 mmol), tributylphenyl tin (2.2 g, 6.07 mmol), bis(triphenylphosphine)palladium (II) chloride (164 mg, 0.234 mmol), and triphenylphosphine (613 mg, 2.34 mmol) in DMF (15 ml) was heated under N2 at 120° C. overnight. After the solution was cooled to room temperature, the reaction mixture was directly chromatographed on silica gel eluting with 2-5% EtOAc/Hexane to give 752 mg (75%) of 5 as a yellow solid: mp 169-171° C.; IR (CHCl3) 3517, 3398, 3022, 1635, 1525, 1250; 1H NMR δ 8.38 (1H, d, J=2.2), 7.66 (1H, dd, J=8.7, 2.2), 7.59-7.54 (2H, m), 7.49-7.34 (3H, m), 6.90 (1H, d, J=8.8), 6.13 (NH, brs); 13C NMR δ 144.2, 139.3, 135.0, 130.9, 129.5, 127.8, 126.8. 124.4, 119.8, 112.8; Anal. Calcd for C12H10N2O2 : C, 67.28; H, 4.70; N, 13.08. Found: C, 67.38, H, 4.76; N, 13.01.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05948797
출처 데이터셋uspto-grants-1999_09
ORD IDord-dbeb5e97e690414f820cb6ba3948b5b6
출처 메모uspto-grants-1999_09