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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356649Generated: November 1, 2026

2-Bromobenzyl bromide → 4-[3-(2-Bromo-4-methoxybenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

https://huagongshe.com/reaction/2356649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl bromideHCID 76965—
Reactant2-Bromo-1-(bromomethyl)-4-methoxybenzeneHCID 10588783—
Reactant4-(4,4-Dimethyl-2,5-dioxoimidazolidin-1-yl)-2-trifluoromethylbenzonitrileHCID 11162285—
Product4-[3-(2-Bromo-4-methoxybenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrileHCID 68678206—

Reaction Steps

Compound 110.2 was prepared as described for example 1.2, by reacting compound 1.1, instead of with 2-bromobenzyl bromide, with 2-bromo-1-bromomethyl-4-methoxybenzene (prepared by N-bromosuccinimide bromination from 2-bromo-4-methoxy-1-methylbenzene; 1H NMR: 7.56, d, 1H, 7.23, s, 1H, 7.0, d, 1H, 4.74, s, 2H; 3.8, s, 3H). 4-[3-(2-Bromo-4-methoxybenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile was obtained. (Molecular weight 495.04 (C21H17BrF3N3O3); 1H NMR: 8.38, d, 1H, 8.25, s, 1H, 8.1, d, 1H, 7.5, d, 1H, 7.22, s, 1H, 6.95, d, 1H, 4.6, s, 2H, 3.79, s, 3H, 1.4, s, 6H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759366B2
Source datasetuspto-grants-2010_07
ORD IDord-cc9225f1ab834b1c9c08a2b6afab3f26
Source noteuspto-grants-2010_07