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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1656644생성일: 2026년 10월 26일

1,2,3,4-Tetrahydro-1-naphthylamine → N-(1,2,3,4-tetrahydronaphth-1-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine

https://huagongshe.com/reaction/1656644

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-Tetrahydro-1-naphthylamineHCID 18066—
반응물2-Naphthyl glycidyl etherHCID 92995—
생성물N-(1,2,3,4-tetrahydronaphth-1-yl)-2-hydroxy-3-(2-naphthyloxy)propanamineHCID 4875225—

반응 단계

Following the general procedure of Example 98, but starting from 1-(2-naphthyloxy)-2,3-epoxypropane (4.5 g) and 1-aminotetralin (2.95 g), N-(1,2,3,4-tetrahydronaphth-1-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine free base is obtained as an oily product which is dissolved in an isopropyl ether/isopropanol 1/1 mixture (40 ml) and acidified with HC1/isopropanol. The corresponding hydrochloride is thus obtained which is crystallized from isopropanol (20 ml). Yield: 2.2 g; m.p. 135°-137° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05254595
출처 데이터셋uspto-grants-1993_10
ORD IDord-a093b90a64b948ad8fd601b1ee79d107
출처 메모uspto-grants-1993_10