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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653677Generated: October 27, 2026

O-Methyltyramine → 2-[(4-Methoxyphenethyl)aminomethyl]-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1653677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethyltyramineHCID 4657—
Reactant2-(Bromomethyl)-1,2,3,4-tetrahydronaphthaleneHCID 12723282—
SolventEthanolHCID 702—
Product2-[(4-Methoxyphenethyl)aminomethyl]-1,2,3,4-tetrahydronaphthaleneHCID 981764059%

Reaction Steps

A solution of 2-bromomethyl-1,2,3,4-tetrahydronaphthalene (1.33 g, 5.91 mmol) and 4-methoxyphenethylamine (1.79 g, 11.8 mmol) in 50 ml of EtOH was refluxed for 48 hours. After removal of EtOH in vacuo, the residue was dissolved in 100 ml of CHCl3, washed with 10% K2CO3, H2O, sat'd brine, and then dried over Na2SO4. Filtration followed by evaporation of solvent gave a yellow oil, which was purified by chromatography (SiO2, MeOH:CHCl3, 5:95) to a give a yellowish oil (1.03 g, 58.9%). The product was converted to HCl salt, crystallization with MeOH/Et2O gave a white powder. mp 274°-275° C.; Calcd for C20H25NO.HCl: C 72.37, H 7.91,N 4.22; Found C 72.40, H 7.76,N 4.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403847
Source datasetuspto-grants-1995_04
ORD IDord-54e059e1ce814d27b7c2d7dfea3190b0
Source noteuspto-grants-1995_04