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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422425Generated: October 28, 2026

Imidazole → 3-(1H-Imidazol-1-yl)propane-1,2-diol

https://huagongshe.com/reaction/1422425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium IodideHCID 4875—
Reactant3-Chloro-1,2-propanediolHCID 7290—
ReactantPotassium HydroxideHCID 14797—
SolventAcetonitrileHCID 6342—
Product3-(1H-Imidazol-1-yl)propane-1,2-diolHCID 301571396%

Reaction Steps

Imidazole (3.40 g, 50.0 mmol), pulverized potassium hydroxide (5.61 g, 100 mmol), and potassium iodide (8.30 g, 50.0 mmol) were suspended in CH3CN (100 mL). 3-Chloro-1,2-propanediol (8.29 g, 75.0 mmol) was added, and the mixture was stirred at reflux for 24 h. After cooling to room temperature, additional CH3CN (150 mL) was added to the reaction, which was then filtered through Celite and concentrated. The crude product was then suspended in CH2Cl2 (250 mL), heated to reflux and stirred overnight, and then decanted. The product was still slightly impure by 1H NMR, so the CH2Cl2 wash process was repeated once, to afford a white solid (6.82 g, 96%) after drying in vacuo. 1H NMR (400 MHz, DMSO) δ 7.54 (t, J=1.0 Hz, 1H), 7.11 (t, J=1.2 Hz, 1H), 6.84 (t, J=1.0 Hz, 1H), 5.08 (s, 1H), 4.83 (s, 1H), 4.05 (dd, J=13.9, 3.6 Hz, 1H), 3.84 (dd, J=14.0, 7.2 Hz, 1H), 3.70-3.58 (m, 1H), 3.31 (dt, J=13.8, 9.0 Hz, 3H), 3.19 (dd, J=11.0, 6.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08926732B2
Source datasetuspto-grants-2015_01
ORD IDord-bd74e8451bf14900a67e832ee217a0aa
Source noteuspto-grants-2015_01