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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711254Generated: October 26, 2026

1-(4-Bromo-3-nitrophenyl)ethan-1-one → 1-[4-(4,4-Dimethyl-cyclohex-1-enyl)-3-nitro-phenyl]-ethanone

https://huagongshe.com/reaction/1711254

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromo-3-nitrophenyl)ethan-1-oneHCID 87737—
Reactant4,4-Dimethylcyclohexen-1-ylboronic acidHCID 44119555—
SolventEthyl acetate hexaneHCID 21226206—
Product1-[4-(4,4-Dimethyl-cyclohex-1-enyl)-3-nitro-phenyl]-ethanoneHCID 5875481399.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790724B2
Source datasetuspto-grants-2010_09
ORD IDord-61e10964513f49659af0071a7f74411b
Source noteuspto-grants-2010_09