HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Bromo-3-nitrophenyl)ethan-1-one → 1-[4-(4,4-Dimethyl-cyclohex-1-enyl)-3-nitro-phenyl]-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Bromo-3-nitrophenyl)ethan-1-one | HCID 87737 | — |
| Reactant | 4,4-Dimethylcyclohexen-1-ylboronic acid | HCID 44119555 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 1-[4-(4,4-Dimethyl-cyclohex-1-enyl)-3-nitro-phenyl]-ethanone | HCID 58754813 | 99.2% |
Reaction Steps
The title compound was prepared by the Suzuki coupling procedure of Example 11, step (e) using 1-(4-bromo-3-nitro-phenyl)-ethanone (347 mg, 1.42 mmol), and 4,4-dimethylcyclohexen-1-ylboronic acid (254 mg, 1.65 mmol). Silica gel chromatography (5-15% EtOAc/hexane) afforded the title compound (385 mg, 99%) as a faint green oil. Mass spectrum (APCI, m/z): Calcd. for C16H19NO3, 274.1 (M+H), found 274.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790724B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-61e10964513f49659af0071a7f74411b |
| Source note | uspto-grants-2010_09 |