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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656632Generated: November 1, 2026

Ethanol → 2-Aminotetralin

https://huagongshe.com/reaction/1656632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 19788355HCID 19788355—
SolventHCID 19788274HCID 19788274—
Product2-AminotetralinHCID 34677—

Reaction Steps

Following the procedure of Example 27, but starting from 1-acetyl-5-(2,3-epoxypropoxy)-1,2,3,4-tetrahydroquinoline (2.77 g) and 2-aminotetralin (1.49 g) in ethanol (30 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(1-acetyl-1,2,3,4-tetrahydroquinolin-5-yloxy)propanamine hydrochloride is obtained ((i): R=H, Ar=radical 66, 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-544e3145d5f84447be20b9f3f6d8b044
Source noteuspto-grants-1993_10