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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2237생성일: 2026년 10월 23일

P-Anisidine → N-(4-methoxyphenyl)pyridin-4-amine

https://huagongshe.com/ko/reaction/2237

반응식

참여 물질

역할이름HCID투입량
반응물P-AnisidineHCID 7732—
반응물4-Chloropyridine hydrochlorideHCID 81852—
용매DichloromethaneHCID 6344—
생성물N-(4-methoxyphenyl)pyridin-4-amineHCID 3628677—

반응 조건

온도140 °C

반응 단계

A stirred mixture of 4-chloropyridine hydrochloride (2 g) and 4-methoxyaniline (4.9 g) was heated at 140° C. for 5 hours. After cooling the residue was dissolved in dichloromethane (250 ml), the solution extracted with water (2×100 ml). The aqueous extracts were treated with sodium hydroxide solution and then extracted with ethyl acetate (4×100 ml). The combined organic extracts were washed with water, and saturated sodium chloride solution, then dried and the solvent evaporated. Purification by flash chromatography on silica, eluting with 10% v/v methanol/dichloromethane gave 4-(4-pyridylamino)-methoxybenzene, 2 g, as a fawn solid: m.p. 159°-160° C.; NMR (d6DMSO) δ8.47 (1H, s), 8.09 (2H, d), 7.10 (2H, d), 6.92 (2H, d), 6.70 (2H, dd), 3.73 (3H, s); m/e 201 (M+H)+ ; calculated for C12H12 N2O3 : C, 72.0; H, 6.0; N, 14.0. found: C, 71.4; H, 6.1; N, 13.8%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728701
출처 데이터셋uspto-grants-1998_03
ORD IDord-88019f4b8c9b42769694053eccb9f705
출처 메모uspto-grants-1998_03