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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1078071생성일: 2026년 10월 26일

Bis(2-Methoxyethyl)amine → 1,2,3,4-Tetrahydro-8-methoxy-N,N-bis(2-methoxyethyl)-2-naphthalenamine

https://huagongshe.com/reaction/1078071

반응식

참여 물질

역할이름HCID투입량
반응물Bis(2-Methoxyethyl)amineHCID 2383—
반응물8-Methoxy-3,4-dihydronaphthalen-1(2H)-oneHCID 11275335—
촉매p-Toluenesulfonic acidHCID 6101—
용매TolueneHCID 1140—
생성물1,2,3,4-Tetrahydro-8-methoxy-N,N-bis(2-methoxyethyl)-2-naphthalenamineHCID 1833180480%

반응 단계

A solution of 1.76 g (10 mmol) 8-methoxy tetralone, 2.66 g (20 mmol) N,N-bis(-2methoxyethyl)amine, and 25 mg p-toluenesulfonic acid in toluene was heated to reflux under a N2 atmosphere. The flask was equipped with a Dean-Stark trap to collect H2O. TLC analysis was used to monitor the reaction. After 48 hours, the solvent was removed in vacuo. The crude ene-amine was hydrogenated using 450 mg 10% pd/C in 50 mL MeOH at 50 psi H2 for 24 hours. The reaction mixture was filtered over celite and the filtrate purified by liquid chromatography on 400 g of silica gel-60 (230-400 mesh), eluting with hexane/ethyl acetate/isopropanol (10:5:1). Fractions homogeneous by TLC were combined and concentrated in vacuo to give pure title compound as a yellow oil (2.3 g, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05545755
출처 데이터셋uspto-grants-1996_08
ORD IDord-bd3701025fd141bbb1cf73490c632a8e
출처 메모uspto-grants-1996_08