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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-Chloro-1,2-propanediol | HCID 7290 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(1H-Imidazol-1-yl)propane-1,2-diol | HCID 3015713 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08926732B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-bd74e8451bf14900a67e832ee217a0aa |
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| Source note | uspto-grants-2015_01 |
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