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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643213Generated: October 28, 2026

Iodine → HCID 66757302, compound

https://huagongshe.com/reaction/1643213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Butyl-4-phenyl-1H-imidazoleHCID 18437789—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66757302HCID 66757302—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-butyl-4-phenylimidazole (4.0 g, 20 mmol) in 60 ml of anhydrous THF at −78° C. under nitrogen is added a solution of n-butyllithium in hexane (1.6M, 13.13 ml, 21 mmol, 1.05 eq.) dropwise. The resulting mixture is stirred at −78° C. for 1 h followed by dropwise addition of a solution of iodine (5.33 g, 21 mmol, 1.05 eq.) in 40 ml of THF. The resulting solution is stirred at −78° C. for 30 min. and then warmed to room temperature. Saturated ammonium chloride (30 mL) is added to quench the reaction. The resulting mixture is evaporated a reduced pressure to remove THF, extracted with ethyl acetate, washed with water and brine, dried over Na2-SO4, filtered and evaporated. Purification by silica gel chromatography (hexanes/ethyl acetate, from 8:1 to 5:1) affords 5.73 g of butyl-2-iodo-4-phenylimidazole. 1H NMR (400 MHz, CDCl3) δ 7.73 (2H, dd, J=1.2, 8.4 Hz), 7.36 (2H, m), 7.30 (1H, s), 7.24 (1H, m), 3.91 (2H, t, J=7.2 Hz), 179 (2H, m), 1.41 (2H, m), 0.98 (3H, t, J=7.2Hz); MS (+VE) m/z 327 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119665B2
Source datasetuspto-grants-2012_02
ORD IDord-9e69feb8b06447eabd220495d9f384f1
Source noteuspto-grants-2012_02