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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 855913생성일: 2026년 10월 25일

2-Amino-m-cresol → 2-[(5-Methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol

https://huagongshe.com/reaction/855913

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-m-cresolHCID 3014138—
반응물5-Methoxy-2-(methoxymethoxy)benzaldehydeHCID 11435522—
용매BenzeneHCID 241—
생성물2-[(5-Methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenolHCID 2195932384%

반응 단계

A solution of 5-methoxy-2-methoxymethoxybenzaldehyde (F1) (2.77 g, 16.5 mmol) and 2-amino-m-cresol (2.03 g, 16.5 mmol) in benzene (70 mL) was refluxed for 15 h using an additional funnel to remove water. After the reaction mixture was cooled to room temperature, the solvent was removed in vacuo and the resulting residue was washed with ethanol to afford the objective compound as a orange solid (84%), which was used for next reaction without further purification: 1H-NMR (400 MHz, DMSO-d6) δ2.31 (s, 3H), 3.45 (s, 3H), 3.85 (s, 3H), 5.18 (s, 2H), 6.59 (s, 1H), 6.77 (d, 1H, J=8.0 Hz), 6.83 (d, 1H, J=8.0 Hz), 6.99 (t, 1H, J=8.0 Hz), 7.03 (dd, 1H, J=9.0, 2.5 Hz), 7.14 (d, 1H, J=9.0 Hz), 7.68 (s, 1H), 8.95 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07262301B1
출처 데이터셋uspto-grants-2007_08
ORD IDord-58bf8e89abbc4638a914503d9c57587d
출처 메모uspto-grants-2007_08