HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2,4,6-Tris(1-methylethyl)phenyl)ethan-1-one → HCID 15725271, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2,4,6-Tris(1-methylethyl)phenyl)ethan-1-one | HCID 75224 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15725271 | HCID 15725271 | 100% |
Reaction Steps
To a solution of 1 (2,4,6-triisopropylphenyl)ethanone (10.0 g, 65.3 mmol) in acetonitrile (81 mL) was added tetrabutylammoniumtribromide (TBABr3, 19.6 g, 40.6 mmol). The reaction was stirred at room temperature for 3.0 h. 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-(2,4,6-triisopropylphenyl)ethanone (13.2 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-63817e0df10e481cae89ab9acd484175 |
| Source note | uspto-grants-2015_04 |