HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzyloxy-2,3-difluoro-6-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Difluoro-6-nitrophenol | HCID 2733745 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyloxy-2,3-difluoro-6-nitrobenzene | HCID 17858881 | 97% |
Reaction Steps
A mixture of 2,3-difluoro-6-nitrophenol (15.1 g), benzyl bromide (10.8 mL) and potassium carbonate (11.9 g) in N,N-dimethylformamide (60 mL) was stirred at room temperature for 15 h. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with successively water and brine, dried (MgSO4), filtered, and concentrated to give the title compound (22.1 g, 97%) as a light yellow solid. MS 264 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673942B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-41e1ae67a5af4afab211cac53676dbb3 |
| Source note | uspto-grants-2014_03 |