HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetra-n-butylammonium tribromide → HCID 58442436, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Reactant | HCID 58442556 | HCID 58442556 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58442436 | HCID 58442436 | 100.3% |
Reaction Steps
To a solution of 1-(2,6-dimethyl-4-phenoxyphenyl)ethanone (3.60 g, 15.0 mmol) in acetonitrile (30 mL) was added tetrabutylammoniumtribromide (TBABr3, 7.95 g, 15.0 mmol). The reaction was stirred at room temperature overnight. The solution was concentrated under reduced pressure, added with water, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous MgSO4(s), and concentrated under reduced pressure to give 2-bromo-1-(2,6-dimethyl-4-phenoxyphenyl)ethanone (4.8 g), which was used directly for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999983B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-2349df914312405f8b12db247379c712 |
| Source note | uspto-grants-2015_04 |