HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 1-Bromo-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-5-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | 3-Bromo-5-fluorophenol | HCID 21904636 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-5-fluorobenzene | HCID 59458554 | 58% |
Reaction Steps
To a solution of 3-bromo-5-fluorophenol (5.7 g, 30 mmol), prepared as described in Procedure 3, and imidazole (4.0 g, 60 mmol, 2 eq) in anhydrous THF (100 mL) at 0° C. was added tert-butyldiphenyl-silyl chloride (9.6 mL, 1.3 eq). The resulting mixture was stirred at room temperature for 18 h. The reaction mixture was quenched with water and extracted with hexane/EtOAc (1:1). The combined organic layers were washed with H2O (2×) and sat. NaCl (2×), dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexanes/EtOAc) to give (3-bromo-5-fluorophenoxy)(tert-butyl)diphenylsilane as colorless oil (7.5 g, yield 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642576B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-51450acd416b4bc29dd58bd8d3c52a60 |
| Source note | uspto-grants-2014_02 |