HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261947Generated: October 26, 2026
Carbon Dioxide → 1-(Methoxymethyl)-alpha-phenyl-alpha-(p-trifluoromethyl-phenyl)imidazole-2-methanol
https://huagongshe.com/reaction/261947
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 4-(Trifluoromethyl)benzophenone | HCID 69767 | — |
| Reactant | 1-(methoxymethyl)-1H-imidazole | HCID 88359 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Methoxymethyl)-alpha-phenyl-alpha-(p-trifluoromethyl-phenyl)imidazole-2-methanol | HCID 12433896 | — |
Reaction Steps
A butyllithium solution, prepared from 1.02 g. (0.145 g. at.) of lithium and 7.9 g. (0.058 mol) of butyl bromide in 70 ml. of anhydrous diethyl ether, was added drop-wise at -60° C. to -65° C. under a nitrogen atmosphere to a solution of 4.9 g. (0.044 mol) of 1-(methoxymethyl)imidazole and 3.1 g. (0.044 mol) of N,N,N',N'-tetramethylethylenediamine in 125 ml. of anhydrous tetrahydrofuran. The reaction mixture was kept standing for 2 hours at -60° to -65° C. and then 11 g. (0.044 mol) of 4-(trifluoromethyl)benzophenone, dissolved in 75 ml. of anhydrous tetrahydrofuran, were added drop-wise. The temperature was maintained at -65° C. for one hour and then the reaction mixture was allowed to attain room temperature overnight. 10 ml. of water and solid carbon dioxide were added and the solvent was distilled off. The residue was dissolved in dilute hydrochloric acid, the solution was washed with diethyl ether and made alkaline with potassium carbonate. The solid substance formed was filtered off and dissolved in chloroform. The solution was washed with water, dried over sodium sulphate and concentrated by evaporation of the solvent. The residue was crystallised from isopropyl alcohol. 1-(Methoxymethyl)-α-phenyl-α-(p-trifluoromethyl-phenyl)imidazole-2-methanol was obtained. Melting point 158°-159° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04152441 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-64f5f377bbfb4dfb8287992cb8ab85b3 |
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| Source note | uspto-grants-1979_05 |
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