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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847028Generated: October 30, 2026

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

https://huagongshe.com/reaction/847028

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=8 Hz); 7.15 (d, 2H, J=8 Hz); 5.26 (s, 2H); 4.25 (s, 2H); 3.23 (s, 3H); 2.52 (t, 2H, J=7 Hz); 1.64 (t of t, 2H, J=7,7 Hz); 1.28 (t of q, 2H, J=7,7 Hz); 0.81 (t, 3H, J=7 Hz). 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 numberUS05138069
Source datasetuspto-grants-1992_08
ORD IDord-a41b312363da4af998da75fa22510025
Source noteuspto-grants-1992_08