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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653867Generated: October 27, 2026

Methanol → 2-n-Butyl-4-chloro-5-methoxymethyl-1-(4-nitrobenzyl)imidazole

https://huagongshe.com/reaction/653867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-hydroxymethyl imidazoleHCID 15356443—
Product2-n-Butyl-4-chloro-5-methoxymethyl-1-(4-nitrobenzyl)imidazoleHCID 53764938—

Reaction Steps

2-n-butyl-4-chloro-5-hydroxymethyl-1-(4-nitrobenzyl)imidazole (10.5 g, 32.4 mmol, 1 eq), conc. sulfuric acid (26 mL) and methanol (300 mL) were mixed and refluxed overnight. The solvent was removed in vacuo and the residue taken up in water (about 300 mL). The pH was adjusted to 5 with 1N NaOH and then this aqueous portion extracted with ethyl acetate (3×250 mL). The organic layers were collected, dried (MgSO4) and the solvent removed in vacuo to yield 11.57 g of an amber oil. NMR (200 MHz, CDCl3) δ 8.22 (d, 2H, J=8Hz); 7.15 (d, 2H, J=8Hz); 5.26 (s, 2H); 4.25 (s, 2H); 3.23 (s, 3H); 2.52 (t, 2H, J=7Hz); 1.64 (t of t, 2H, J=7,7Hz); 1.28 (t of q, 2H, J=7,7Hz); 0.81 (t, 3H, J=7Hz). Anal. Calcd. for C16H20ClN3O3.(H2O)0.5 : C, 55.41; H, 6.10; Cl, 10.22. Found: C, 55.21; H, 6.22; Cl, 9.92.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128355
Source datasetuspto-grants-1992_07
ORD IDord-6e6885d9ec0241c8815bf7c60c70c467
Source noteuspto-grants-1992_07