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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656615Generated: November 2, 2026

Ethanol → 2-Aminotetralin

https://huagongshe.com/reaction/1656615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 19788308HCID 19788308—
SolventHCID 14750955HCID 14750955—
Product2-AminotetralinHCID 34677—

Reaction Steps

Following the procedure described in Example 27, but starting from 2,3-dimethyl-4-(2,3-epoxypropoxy)indole (10 g) and 2-aminotetralin (6.9 g) in ethanol (100 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2,3-dimethylindol-4-yloxy)propanamine hydrochloride is obtained ((i): R=H, Ar=radical 14 wherein Z is methyl, and the chain is attached to position 2 of the tetralin moiety).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254595
Source datasetuspto-grants-1993_10
ORD IDord-cc4f3417359f43409bf7d11ccf2a83d9
Source noteuspto-grants-1993_10