HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638051Generated: October 30, 2026
Isopropyl iodide → HCID 20255183, compound
https://huagongshe.com/reaction/638051
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178488961 | HCID 178488961 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20255183 | HCID 20255183 | — |
Reaction Steps
At an internal temperature of 0°-50°, 10 g of potassium tert.-butoxide are added to a solution of 20 g of 2-(4-methoxyphenyl)-4-(trifluoromethyl)-1H-imidazole in 200 ml of dimethylformamide. After 20 minutes 10.7 ml of isopropyl iodide are added and the reaction mixture is subsequently stirred at room temperature. After 24 hours in each case, a further 10 g of potassium tert.-butoxide are added and then 10.7 ml of isopropyl iodide. In total, these measures are repeated three times. The total reaction period is 120 hours. Finally, the solvent is removed in a rotary evaporator, the residue is taken up in water and extracted several times with ethyl acetate. After evaporating off the organic phase, the residue is chromatographed on silica gel with ethyl acetate/hexane and 2-(4-methoxyphenyl)-1-isopropyl-4-(trifluoromethyl)-1H-imidazole is isolated from the main fractions in the form of a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04559354 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-c3ebd565081543c18a78102c0f691f3f |
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| Source note | uspto-grants-1985_12 |
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