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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576079Generated: October 25, 2026

Isopropanol → 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline

https://huagongshe.com/reaction/576079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant4-Bromo-2-fluoroanilineHCID 123050—
Reactant(2-Cyclohexylvinyl)boronic acidHCID 6031024—
ReactantHCID 178418922HCID 178418922—
Catalyst1-IodopropaneHCID 33643—
SolventWaterHCID 962—
Product4-[(E)-2-cyclohexylethenyl]-2-fluoroanilineHCID 8670728299.7%

Reaction Steps

Isopropanol (60 mL) was added to PEPPSI™-IPr catalyst (161 mg, 0.24 mmol) and tert-butoxy potassium (2.65 g, 23.6 mmol) under an argon atmosphere, and the mixture was stirred at room temperature for 15 min. To the reaction mixture were added trans-(2-cyclohexylvinyl)boronic acid (2.00 g, 13.0 mmol) and 4-bromo-2-fluoroaniline (2.24 g, 11.8 mmol) successively and the mixture was stirred at room temperature for 15 hr. Water was added thereto, the mixture was extracted with ethyl acetate, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure to afford 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline as a reddish brown oil (2.58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035059B2
Source datasetuspto-grants-2015_05
ORD IDord-c09a1b39f8f547cabadb0c5a76a78547
Source noteuspto-grants-2015_05