HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254542Generated: October 25, 2026
Potassium Iodide → 4-(1-benzyl-1H-imidazol-2-ylmethyl)-heptane-3,5-dione
https://huagongshe.com/reaction/254542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3,5-Heptanedione | HCID 81923 | — |
| Reactant | 1-benzyl-2-(chloromethyl)-1H-imidazole | HCID 736792 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-benzyl-2-(chloromethyl)-1H-imidazole hydrochloride | HCID 2779243 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(1-benzyl-1H-imidazol-2-ylmethyl)-heptane-3,5-dione | HCID 58951861 | 31.5% |
Reaction Steps
To a solution of 1.74 ml (4.7 mmol; ˜21% solution in ethanol) sodium ethanolate in 18 ml dry ethanol were added 600 mg (4.7 mmol) 3,5-heptanedione and stirred at ambient temperature for 30 min. Then a solution of 1-benzyl-2-chloromethyl-1H-imidazole (prepared from 1.081 g (4.5 mmol) 1-benzyl-2-chloromethyl-1H-imidazole hydrochloride in 7 ml ethanol and 1.74 ml (5 mmol; ˜21% solution in ethanol) sodium ethanolate) was added together with 30 mg potassium iodide. The mixture was heated to 50° C. for 10 min and then immediately cooled to ambient temperature and concentrated under reduced pressure at max. 30° C. Purification by flash-chromatography on silica gel with heptane/ethyl acetate 1:1 as eluent provided 423 mg 4-(1-benzyl-1H-imidazol-2-ylmethyl)-heptane-3,5-dione as light brown oil: MS (ISP): 299.2 ((M+H)+.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07875645B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-f45ec7e7b62747a79a67191e786acfef |
|---|
| Source note | uspto-grants-2011_01 |
|---|