HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → ((3-Bromo-5-nitrobenzyl)oxy)(tert-butyl)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (3-Bromo-5-nitrophenyl)methanol | HCID 14866972 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ((3-Bromo-5-nitrobenzyl)oxy)(tert-butyl)dimethylsilane | HCID 67431768 | 93.5% |
Reaction Steps
A solution of 3-bromo-5-nitrobenzyl alcohol (5 g, 21.5 mmol), in N,N-dimethylformamide (5 mL) was treated with tert-butyldimethylsilyl chloride (4.9 g, 32.3 mmol) and imidazole (2.5 g, 36.6 mmol) and stirred at room temperature for 14 h. The reaction was quenched with water and extracted with ethyl acetate (2×). The organic layer was dried over sodium sulfate, filtered, and concentrated. Purification by flash chromatography on silica (0-75% ethyl acetate in hexanes) afforded [(3-bromo-5-nitrobenzyl)oxy](tert-butyl)dimethylsilane (7.32 g, 20.1 mmol, 93% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759366B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-02d77ed9143d4fda8cea5d789f2aa38f |
| Source note | uspto-grants-2014_06 |