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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711259Generated: November 2, 2026

Ethyl Acetate → 4-Bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenylamine

https://huagongshe.com/reaction/1711259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-iodoanilineHCID 823934—
Reactant4,4-Dimethylcyclohexen-1-ylboronic acidHCID 44119555—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product4-Bromo-2-(4,4-dimethyl-cyclohex-1-enyl)-phenylamineHCID 5912857193.8%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-04784639bf524eb88f4963f3c16ce653
Source noteuspto-grants-2010_09