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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1656643생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1656643

반응식

참여 물질

역할이름HCID투입량
반응물2-AminotetralinHCID 34677—
반응물2-Naphthyl glycidyl etherHCID 92995—
용매EthanolHCID 702—
생성물N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamineHCID 1978825253.2%

반응 단계

A mixture of 1-(2-naphthyloxy)-2,3-epoxypropane (1.95 g), 2-aminotetralin (2.65 g) and ethanol (35 ml) is heated to the reflux temperature for 5 hours. The solvent is then evaporated off and the thus obtained solid residue is crystallized from ethyl acetate (5 ml), recovered by filtration, washed with ethyl acetate and then with ethyl ether, and dried yielding 1.8 g of N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine, as the free base; m.p. 102°-115° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05254595
출처 데이터셋uspto-grants-1993_10
ORD IDord-6d61e845ef5d45ed9a722e30b04140de
출처 메모uspto-grants-1993_10