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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656643Generated: October 27, 2026

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

https://huagongshe.com/reaction/1656643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminotetralinHCID 34677—
Reactant2-Naphthyl glycidyl etherHCID 92995—
SolventEthanolHCID 702—
ProductN-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamineHCID 1978825253.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254595
Source datasetuspto-grants-1993_10
ORD IDord-6d61e845ef5d45ed9a722e30b04140de
Source noteuspto-grants-1993_10