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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956399Generated: October 27, 2026

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

https://huagongshe.com/reaction/1956399

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 numberUS05780485
Source datasetuspto-grants-1998_07
ORD IDord-493ff2ded6c5493bb1e564e6995305ce
Source noteuspto-grants-1998_07