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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878771Generated: October 27, 2026

Hexane → (4-Bromophenyl)[1-(trifluoromethyl)cyclopropyl]methanone

https://huagongshe.com/reaction/878771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-methoxy-N-methyl-1-(trifluoromethyl)cyclopropane-1-carboxamideHCID 57785368—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromophenyl)[1-(trifluoromethyl)cyclopropyl]methanoneHCID 6828972876%

Reaction Steps

To a solution of 4-bromoiodobenzene (2150 mg, 7.60 mmol) in tetrahydrofuran (20 mL) was added dropwise a solution of 1.67 mol/L n-butyllithium in hexane (4.50 mL, 7.52 mmol) at −78° C. under argon atmosphere. The mixture was stirred at the same temperature for 1 hour, and then thereto was added dropwise a solution of N-methoxy-N-methyl-1-(trifluoromethyl)cyclopropanecarboxamide (synthesized by the method of Organic Process Research and Development 2009, 13, 576, 1000 mg, 5.07 mmol) in tetrahydrofuran (10 mL), and the mixture was stirred at the same temperature for 1 hour. To the reaction solution was added saturated aqueous ammonium chloride solution at −78° C., and then the mixture was warmed to room temperature and extracted with ethyl acetate three times. The organic layer was combined, washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0→95:5) to give (4-bromophenyl)[1-(trifluoromethyl)cyclopropyl]methanone (783 mg, 76%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987445B2
Source datasetuspto-grants-2015_03
ORD IDord-a3307ea0bcdf411da55d814482c13605
Source noteuspto-grants-2015_03