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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1018748생성일: 2026년 10월 25일

Triethylamine → N-(9-Acridinyl)-4-(7-hydroxyheptyl)-aniline

https://huagongshe.com/reaction/1018748

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물9-ChloroacridineHCID 71013—
반응물4-(7-Hydroxyheptyl)-anilineHCID 22647796—
용매MethanolHCID 887—
생성물N-(9-Acridinyl)-4-(7-hydroxyheptyl)-anilineHCID 2264781791.4%

반응 단계

To a solution of 636.9 mg (3.07 mmol) of 4-(7-hydroxyheptyl)-aniline 30 and 428 μL (3.07 mmol) of Et3N in 20 mL of MeOH were added 656.4 mg (3.07 mmol) of 9-chloroacridine. After stirring for 7 hr at room temperature, the solvent was evaporated. Purification by column chromatography on silica gel with 5% MeOH in CH2Cl2 gave 1.079 g (91%) of N-(9-acridinyl)-4-(7-hydroxyheptyl)-aniline 31: 1H NMR (300 MHz, CDCl3, TMS) δ8.0-7.9 (m, 4H), 7.63 (t, J=7 Hz, 2H), 7.3-7.2 (m, 2H), 7.07 (d, J=8.3 Hz, 2H), 6.85 (d, J=8.3 Hz, 2H), 3.64 (t, J=6.6 Hz, 2H), 2.57 (t, J=7.6 Hz, 2H), 1.7-1.5 (m, 4H), 1.4-1.3 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06482943B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-826a1b4170634328b0eb97d9fffbb895
출처 메모uspto-grants-2002_11