Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 2-Bromoanisole | HCID 11358 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 5305516 | HCID 5305516 | 50% |
Reaction Steps
To a degassed DMSO (20 mL) solution of imidazole (1.0 g, 15 mmol) was added 2-bromoanisole (1.25 mL, 10 mmol), KOH (1.12 g, 20 mmol) and Cu2O (280 mg, 2 mmol) under nitrogen. The resulting mixture was stirred at 140° C. for 24 hrs under N2. After cooling to room temperature, the mixture was poured into ethylacetate (EA) (50 mL) and filtered. The filtrate was washed with water (50 mL×3) and dried over anhydrous magnesium sulfate. After rotary evaporation, the crude oil was purified via column chromatography on silica gel with eluent of EA/MeOH (9/1, v/v), affording a light yellow liquid (50%). 1H-NMR (400 MHz, CDCl3) δ(ppm) 7.79 (s, 1H), 7.36 (t, J=7.8 Hz, 1H), 7.28 (d, J=7.8 Hz, 1H), 7.21 (s, 1H), 7.17 (s, 1H), 7.05 (m, 2H), 3.85 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08957217B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-359cad5590ec4dce85078c3586731dda |
|---|
| Source note | uspto-grants-2015_02 |
|---|