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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656642Generated: November 1, 2026

1-(1-Phenyltetrazol-5-yloxy)-2,3-epoxypropane → 2-Aminotetralin

https://huagongshe.com/reaction/1656642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Phenyltetrazol-5-yloxy)-2,3-epoxypropaneHCID 12399823—
SolventEthanolHCID 702—
SolventN-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(1-phenyltetrazol-5-yloxy)propanamine hydrochlorideHCID 14751089—
Product2-AminotetralinHCID 34677100.4%

Reaction Steps

Following the procedure of Example 27, but starting from 1-(1-phenyltetrazol-5-yloxy)-2,3-epoxypropane (4.37 g) prepared as described in BE 866,278 and 2-aminotetralin (1.48 g) in absolute ethanol (60 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(1-phenyltetrazol-5-yloxy)propanamine hydrochloride is obtained ((i): R=H, Ar=radical 60, wherein Z=Z'=H 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-76719bc6329946e595c2f6941802a886
Source noteuspto-grants-1993_10