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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406227Generated: October 31, 2026

Imidazole → 4'-Chloro-2-(iodomethyl)biphenyl

https://huagongshe.com/reaction/2406227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(4-Chlorophenyl)benzyl alcoholHCID 1392780—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
Product4'-Chloro-2-(iodomethyl)biphenylHCID 6705429355%

Reaction Steps

Triphenylphosphine (8.47 g, 32.3 mmol), iodine (8.94 g, 35.2 mmol), imidazole (2.40 g, 352 mmol), and CH2Cl2 (110 mL) were combined in a round-bottom flask, and the mixture was stirred for 15 minutes. A solution of (4′-chloro-biphenyl-2-yl)-methanol in CH2Cl2 (40 mL) was then added, and the reaction was stirred at room temperature for 16 hours (flask was wrapped in aluminum foil to shield it from the light). A saturated aqueous Na2S2O2 was added. The layers were separated, and the aqueous layer was extracted with CH2Cl2 (2×100 mL). The organic layers were combined, dried over MgSO4, and concentrated. The crude residue was purified by flash chromatography on silica gel (0-10% EtOAc/heptanes) to afford the title compound as an off-white solid (5.33 g, 55% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.51-7.53 (m, 1H), 7.38-7.46 (m, 4H), 7.28-7.37 (m, 2H); 7.15-7.17 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809352B2
Source datasetuspto-grants-2014_08
ORD IDord-d6d20621b1624f64bfa8fe3b53015dba
Source noteuspto-grants-2014_08