HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455992Generated: October 26, 2026
Ethyl Acetate → 4-Bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenylamine
https://huagongshe.com/reaction/455992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-2-iodoaniline | HCID 823934 | — |
| Reactant | 4,4-Dimethylcyclohexen-1-ylboronic acid | HCID 44119555 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenylamine | HCID 59128571 | 93.8% |
Reaction Steps
A mixture of 4-bromo-2-iodo-phenylamine (873 mg, 2.93 mmol), 4,4-dimethylcyclohexen-1-ylboronic acid (496 mg, 3.22 mmol), Pd(PPh3)4 (169 mg, 0.147 mmol) and 2.0 M aq Na2CO3 (11.7 mL, 23.4 mmol) in 20 mL of 1,4-dioxane was stirred at 80° C. for 12 h under Ar. After cooling to RT, the reaction was treated with EtOAc (50 mL) and washed with H2O (25 mL) and brine (20 mL). The organic layer was dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (5% EtOAc/hexane) to afford 770 mg (91%) of the title compound as a colorless oil. Mass spectrum (ESI, m/z): Calcd. for C14H18BrN, 280.1 (M+H), found 280.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08497376B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-61ad5578ff83413dbc7e6f5e48da0832 |
|---|
| Source note | uspto-grants-2013_07 |
|---|