HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 4-Bromophenyl-tert-butyldimethylsilyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromophenyl-tert-butyldimethylsilyl ether | HCID 68801317 | — |
Reaction Steps
4-Bromophenol (5.76 g, 30 mmol), imidazole (4.08 g, 60 mmol) and tert-butyldimethylsilyl chloride (5.02 g, 33 mmol) were stirred in anhydrous DMF (100 mL) at 25° C. for 18 h. The reaction mixture was then poured into water (100 mL) and extracted with ethyl acetate (2×75 mL). The combined extracts were washed with water (2×75 mL), brine (75 mL) and dried (MgSO4) before concentration in vacuo. The crude product was purified using "flash" silica gel column chromatography with ethyl acetate:hexane (1:4) as eluant to afford the title compound as an oil, 7.9 g, 92%. 1H NMR (CDCl3, 300 MHz): δ7.33 (app. dt, J=9, 3, 1 Hz, 2H), 6.73 (app. dt, J=9, 3, 1 Hz, 2H) 0.98 (s, 9H),0.21 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05703100 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-a553443ca65749b5af4e693f1204cdb2 |
| Source note | uspto-grants-1997_12 |