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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847078Generated: October 31, 2026

2-(Bromomethyl)benzonitrile → HCID 19815336, compound

https://huagongshe.com/reaction/847078

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)benzonitrileHCID 89599—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 19815308HCID 19815308—
SolventDimethylformamideHCID 6228—
ProductHCID 19815336HCID 1981533654.7%

Reaction Steps

To a solution of 1.00 g of 1-(4-hydroxybenzyl)-2-butyl-4-chloro-5-hydroxymethylimidazole in 15 mL of DMF at 25° was added 0.185 g of sodium methylate, and the resulting mixture was stirred at 25° for 0.25 hours. To this mixture was then added a solution of 0.80 g of α-bromo-o-tolunitrile in 5 mL of DMF. The reaction mixture was stirred at 25° for 16 hours. The solvent was removed in vacuo, and the residue dissolved in ethyl acetate. This solution was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Column chromatography on silica gel (elution: 10-25% ethyl acetate/benzene) provided 0.76 g of 1-[4-(2-cyanobenzyloxy)benzyl]-2-butyl-4-chloro-5-hydroxymethylimidazole; NMR (200 MHz, CDCl3): δ7.73-7.59 (m, 3H); 7.44 (m, 1H); 6.96 (s, 4H); 5.23 (s, 2H); 5.14 (s, 2H); 4.50 (d, 2H); 2.57 (t, 2H); 1.66 (quint., 2H); 1.33 (sext., 2H); 0.87 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05138069
Source datasetuspto-grants-1992_08
ORD IDord-0f8eca5da26e442d9ab9c886e1880505
Source noteuspto-grants-1992_08