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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656631Generated: November 2, 2026

Ethanol → 2-Aminotetralin

https://huagongshe.com/reaction/1656631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 19788318HCID 19788318—
SolventHCID 14751007HCID 14751007—
Product2-AminotetralinHCID 34677—

Reaction Steps

Following the procedure of Example 27, but starting from 4-(4-ethoxycarbonyl-1,2,3-thiadiazol-5-yl)-1-(2,3-epoxypropoxy)benzene (2.94 g) and 2-aminotetralin (1.49 g) in absolute ethanol (20 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-[4-(4-ethoxycarbonyl-1,2,3-thiadiazol-5-yl)phenoxy]propanamine hydrochloride is obtained ((i): R=H, Ar=radical 63, wherein Z is a 4-COOC2H5 group, 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-414322dbf5984641a2ea827c63aeafa2
Source noteuspto-grants-1993_10