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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465603Generated: November 3, 2026

Tetra-n-butylammonium tribromide → HCID 58442497, compound

https://huagongshe.com/reaction/1465603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 58442404HCID 58442404—
SolventAcetonitrileHCID 6342—
ProductHCID 58442497HCID 58442497125.2%

Reaction Steps

To a solution of 1-(3,5-dimethyl-(1,1′-biphenyl)-4-yl)ethanone (1.89 g, 8.43 mmol) in acetonitrile (16.9 mL) was added tetrabutylammoniumtribromide (TBABr3, 4.07 g, 8.43 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-(3,5-dimethyl-(1,1′-biphenyl)-4-yl)ethanone (3.2 g), which was used directly for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999983B2
Source datasetuspto-grants-2015_04
ORD IDord-ec981fe67ab744439d710273e5a9e0a6
Source noteuspto-grants-2015_04