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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356648Generated: November 1, 2026

2-Bromobenzyl bromide → HCID 68678328, compound

https://huagongshe.com/reaction/2356648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl bromideHCID 76965—
Reactant2-Bromo-1-(bromomethyl)-4-chlorobenzeneHCID 10613066—
Reactant4-(4,4-Dimethyl-2,5-dioxoimidazolidin-1-yl)-2-trifluoromethylbenzonitrileHCID 11162285—
ProductHCID 68678328HCID 68678328—

Reaction Steps

Compound 109.2 was prepared as described for example 1.2, by reacting compound 1.1, instead of 2-bromobenzyl bromide, with 2-bromo-1-bromomethyl-4-chlorobenzene (prepared by N-bromosuccinimide bromination from 2-bromo-4-chloro-1-methylbenzene; 1H NMR: 7.82, d, 1H; 7.65, s, 1H, 7.5, d, 1H, 4.72, s, 2H). 4-[3-(2-Bromo-4-chlorobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile was obtained. (Molecular weight 498.99 (C20H14BrClF3N3O2); retention time Rt=2.30 min. [B]; MS (ESI): 541.04 (MH++CH3CN).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759366B2
Source datasetuspto-grants-2010_07
ORD IDord-15014b4e47f54e1a89e7705101eb1486
Source noteuspto-grants-2010_07