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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843758Generated: November 1, 2026

Tetra-n-butylammonium tribromide → HCID 58442384, compound

https://huagongshe.com/reaction/1843758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 58442477HCID 58442477—
SolventAcetonitrileHCID 6342—
ProductHCID 58442384HCID 58442384101.2%

Reaction Steps

To a solution of 1-(4-(4-fluorophenoxy)-2,6-dimethylphenyl)ethanone (4.40 g, 17.0 mmol) in acetonitrile (34.1 mL) was added tetrabutylammoniumtribromide (TBABr3, 9.04 g, 18.8 mmol). The reaction was stirred at room temperature overnight. The solution was concentrated under reduced pressure, added with water, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous MgSO4(s), and concentrated under reduced pressure to give 2-bromo-1-(4-(4-fluorophenoxy)-2,6-dimethylphenyl)ethanone (5.8 g), which was used directly for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946268B2
Source datasetuspto-grants-2015_02
ORD IDord-30bef196a72641d8a2c0b01643ba5f17
Source noteuspto-grants-2015_02