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HRID 1656643作成日:2026年10月26日

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

https://huagongshe.com/reaction/1656643

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminotetralinHCID 34677—
反応物2-Naphthyl glycidyl etherHCID 92995—
溶媒EthanolHCID 702—
生成物N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamineHCID 1978825253.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05254595
出典データセットuspto-grants-1993_10
ORD IDord-6d61e845ef5d45ed9a722e30b04140de
出典メモuspto-grants-1993_10