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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631870Generated: November 3, 2026

Benzyl Bromide → Benzyl-[2-(3,4-dimethoxy-phenyl)-ethyl]-amine

https://huagongshe.com/reaction/1631870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHomoveratrylamineHCID 8421—
ReactantTriethylamineHCID 8471—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl-[2-(3,4-dimethoxy-phenyl)-ethyl]-amineHCID 200274—

Reaction Steps

N-benzyl-2-(3,4-dimethoxyphenyl)ethylamine was prepared using a system (FRX200, Syrris Limited) including a microflow reactor. For this purpose, 83 μl (0.5 mmol) of 2-(3,4-dimethoxyphenyl)ethylamine and 5 ml of tetrahydrofuran were added to the first storage unit of the system including the microflow reactor, and then 70 μl (0.5 mmol) of triethylamine was added thereto. Meanwhile, 60 μl (0.5 mmol) of benzyl bromide and 5 ml of tetrahydrofuran were added to the second storage unit of the system. The reactants included in the first and second storage units were transferred through the first and second flow channels to the mixing unit, and then transferred through the third flow channel into the microflow reactor including microchannels. The first and second flow channels could transfer 360 μl (180 μl for each flow channel) of the reactants to the microflow reactor. The microflow reactor was set at a capacity of 250 μl, a temperature of 100° C. and a pressure of 8 bar. The reactants in the first and second storage units were set such that they were passed through the first to third flow channels at a flow rate of 0.05 ml/min and introduced into the microflow reactor. Also, the residence time of the reactants in the microflow reactor was set at 2.5 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791301B2
Source datasetuspto-grants-2014_07
ORD IDord-829a079113d84c6582c2a17f4e17f29f
Source noteuspto-grants-2014_07