Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | o-(Trifluoromethyl)benzaldehyde | HCID 123067 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86751265 | HCID 86751265 | — |
Reaction Steps
To a solution of 1.5 g of imidazole in 30 ml of THF at 0° C., 8.8 ml of a 2.5M solution of n-butyl lithium in hexane were added slowly over about 7 minutes. The reaction mixture became light yellow and cloudy. After 1.5 hours, 4.2 g of 2-trifluoromethylbenzaldehyde were added slowly at about 10° C. The reaction mixture was allowed to warm to room temperature and then stirred at room temperature over the weekend. 2.9 g of trimethylacetyl chloride were added slowly at room temperature and the mixture was stirred over the weekend. Ice was added to quench the reaction and the layers were separated. The organic layer was dried (MgSO4), filtered and concentrated. The residue was put onto a silica gel column and eluted with a 1:1 mixture of hexane:ethyl acetate to yield 1.5 g of N-(1-trimethylacetoxy-2'-trifluoromethylbenzyl)-imidazole in the form of a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05672567 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-4ee6b5144e08403cb584802b0f251f6f |
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| Source note | uspto-grants-1997_09 |
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