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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466390Generated: October 31, 2026

Stannous chloride dihydrate → 1-(4-Aminobenzyl)-2-butyl-4,5-dicyanoimidazole

https://huagongshe.com/reaction/466390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant2-Butyl-4,5-dicyano-1-(4-nitrobenzyl)imidazoleHCID 19815389—
SolventEthanolHCID 702—
Product1-(4-Aminobenzyl)-2-butyl-4,5-dicyanoimidazoleHCID 19815362—

Reaction Steps

A mixture of 2-butyl-4,5-dicyano-1-(4-nitrobenzyl)imidazole (2.00 g, 6.5 mmol, 1 eq), tin dichloride dihydrate (7.30 g, 32.3 mmol, 5 eq) and ethanol (13 mL) was stirred and heated at 70° for 50 minutes. The reaction was terminated by pouring the mixture onto ice and adjusting the pH to 8 with saturated aqueous NaHCO3. The aqueous mixture was extracted with ethyl acetate (3×100 mL) and the organic layers were dried (MgSO4) and concentrated to give a thick amber oil. This oil was flash chromatographed over silica gel in 75:25 to 70:30 hexane/ethyl acetate yielding 330 mg of yellow crystals; m.p. 99.0°-103.5°. NMR (200 MHz, CDCl3) δ 6.97 (d, 2H, J=10 Hz); 6.68 (d, 2H, J=10 Hz); 5.10 (s, 2H); 2.69 (t, 2H, J=7 Hz); 1.72 (t of t, 2H, J=7,7 Hz); 1.38 (t of q, 2H, J=7,7 Hz); 0.91 (t, 3H, J=7 Hz). Mass Calcd. for C16H17N5 : 279.1483. Found: 279.1489.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155118
Source datasetuspto-grants-1992_10
ORD IDord-df696eb174e54ab29bf4f9ca8437bc72
Source noteuspto-grants-1992_10