HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl bromide → HCID 68678328, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | 2-Bromo-1-(bromomethyl)-4-chlorobenzene | HCID 10613066 | — |
| Reactant | 4-(4,4-Dimethyl-2,5-dioxoimidazolidin-1-yl)-2-trifluoromethylbenzonitrile | HCID 11162285 | — |
| Product | HCID 68678328 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759366B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-15014b4e47f54e1a89e7705101eb1486 |
| Source note | uspto-grants-2010_07 |