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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465773Generated: October 30, 2026

Acetic Acid → Methyl 1-(4-aminobenzyl)-2-butyl-4-chloroimidazole-5-acetate

https://huagongshe.com/reaction/465773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 15159734HCID 15159734—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
ProductMethyl 1-(4-aminobenzyl)-2-butyl-4-chloroimidazole-5-acetateHCID 1535644598.5%

Reaction Steps

A mixture of methyl 2-butyl-4-chloro-1-(4-nitrobenzyl)imidazole-5-acetate (5.00 g, 13.7 mmol, 1 eq), iron (2.67 g, 47.8 mmol, 3.5 eq), glacial acetic acid (5.47 mL, 95.3 mmol, 7 eq), and methanol (250 mL) was refluxed for 5.5 hours. The solvent was removed by rotary evaporation. The residue was diluted with water (300 mL) and extracted five times with 300 mL portions of ethyl acetate. The organic layers were dried and concentrated. The residue was flash chromatographed in 75:25 hexane/ethyl acetate over silica gel to give 4.53 g of a golden yellow oil which crystallized after standing for several days. NMR (200 MHz, CDCl3) δ6.72 (d, 2H, J=7 Hz); 6.60 (d, 2H, J=7 Hz); 4.99 (s, 2H); 3.61 (s, 3H); 3.47 (s, 2H); 2.60 (t, 2H, J= 7 Hz); 1.68 (m, 2H); 1.35 (m, 2H); 0.86 (t, 3H, J=7 Hz). Mass spectrum shows M+=335/337. Mass Calcd. for C17H22N3O2Cl: 335.1400. Found: 335.1407.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153197
Source datasetuspto-grants-1992_10
ORD IDord-0ed9a2772f9946519c4b01323f0a44d1
Source noteuspto-grants-1992_10