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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023652Generated: October 30, 2026

Ethyl Acetate → 4-Bromo-2-cyclohex-1-enyl-phenylamine

https://huagongshe.com/reaction/1023652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-iodoanilineHCID 823934—
Reactant2-(Cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 10932675—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product4-Bromo-2-cyclohex-1-enyl-phenylamineHCID 5945754187%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 4-bromo-2-iodo-phenylamine (2.00 g, 6.71 mmol), 2-cyclohex-1-enyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (1.40 g, 6.71 mmol) and Pd(PPh3)4 (388 mg, 0.336 mmol) in 40 mL of 1,4-dioxane was added 2.0 M aq Na2CO3 solution (26.8 mL, 53.7 mmol). After stirring at 80° C. for 5 h under Ar, the reaction was cooled to RT. The mixture was treated with EtOAc (100 mL), washed with H2O (3×30 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 (10-20% EtOAc/hexane) to give 1.47 g (87%) of the title compound as a light brown oil. Mass spectrum (ESI, m/z): Calcd. for C12H14BrN, 252.0 (M+H), found 252.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722718B2
Source datasetuspto-grants-2014_05
ORD IDord-ccf3b1e6055a462d97e396129d930a5b
Source noteuspto-grants-2014_05