HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → Ethyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Ethyl 4-hydroxycyclohexanecarboxylate | HCID 86973 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylate | HCID 23144129 | 100% |
Reaction Steps
Ethyl 4-hydroxycyclohexanecaboxylate (3.44 g, 20.0 mmol) was dissolved in DMF (7 mL), and imidazole (3.40 g, 50.0 mmol) and tert-butyldimethylsilyl chloride (3.62 g, 24 mmol) were added thereto, followed by stirring overnight at room temperature. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=10:1) to afford ethyl 4-(tert-butyldimethylsilyloxy)cyclohexanecarboxylate (5.73 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07880013B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-e8b25028b1d94faa91b5981708d247da |
| Source note | uspto-grants-2011_02 |