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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653893Generated: October 31, 2026

N-bromobutanimide → 1-[(2'-Carbomethoxybiphenyl-4-yl)-methyl]-2-(2-bromobutyl)-4-chloroimidazole-5-carboxaldehyde

https://huagongshe.com/reaction/653893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-(2'-Carbomethoxybiphenyl-4-yl)methyl-2-butyl-4-chloroimidazole-5-carboxaldehydeHCID 15698069—
SolventCarbon TetrachlorideHCID 5943—
Product1-[(2'-Carbomethoxybiphenyl-4-yl)-methyl]-2-(2-bromobutyl)-4-chloroimidazole-5-carboxaldehydeHCID 1988957540.4%

Reaction Steps

A mixture of 1.12 g of 1-[(2'-carbomethoxybiphenyl-4-yl)methyl]-2-butyl-4-chloroimidazole-5-carboxaldehyde and 0.49 g of N-bromosuccinimide in 40 mL of CCl4 was irradiated (UV-lamp, pyrex filter) for 0.5 hours. The reaction mixture was filtered, and the filtrate was concentrated in vacuo. Column chromatography (elution: ethyl acetate/benzene) afforded 0.54 g of 1-[(2'-carbomethoxybiphenyl-4-yl)-methyl]-2-(2-bromobutyl)-4-chloroimidazole-5-carboxaldehyde. NMR (200 MHz, CDCl3) δ 9.87 (s, 1H); 7.86 (d, 1H); 7.54 (t, 1H); 7.46 (t, 1H); 7.30 (m, 3H); 7.11 (d, 2H); 6.16 (d, 1H); 5.32 (d, 1H); 4.79 (t, 1H); 3.65 (s, 3H); 2.32 (m, 2H); 1.34 (sext., 2H); 0.83 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128355
Source datasetuspto-grants-1992_07
ORD IDord-22140c5228334f588318edb2d42bcce7
Source noteuspto-grants-1992_07