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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603731Generated: October 25, 2026

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

https://huagongshe.com/reaction/1603731

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 numberUS05990128
Source datasetuspto-grants-1999_11
ORD IDord-3da913d947c04899a9436a880de8fa1d
Source noteuspto-grants-1999_11