Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 67069911 | HCID 67069911 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67069940 | HCID 67069940 | 83% |
Reaction Steps
step 2—A mixture of 114 (0.20 g, 0.59 mmol), 4-nitrophenol (0.082 g, 0.59 mmol) and K2CO3 (0.12 g, 0.89 mmol) in DMF was stirred at 50° C. for 2 h. The mixture was cooled to RT and partitioned between water and Et2O. The ether layer was concentrated, and the crude residue was purified by SiO2 chromatography eluting with EtOAc/hexane to afford 0.19 g (83%) of 5-bromo-1-tert-butyl-2-methoxy-3-(4-nitro-phenoxymethyl)benzene (116) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273773B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-bf4c0c0ce41246d88e237ab3064687c5 |
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| Source note | uspto-grants-2012_09 |
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