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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465617Generated: October 30, 2026

Tetra-n-butylammonium tribromide → HCID 58442422, compound

https://huagongshe.com/reaction/1465617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 58442531HCID 58442531—
SolventAcetonitrileHCID 6342—
ProductHCID 58442422HCID 58442422100.6%

Reaction Steps

To a solution of 1-(4-(cyclopentyloxy)-2,6-dimethylphenyl)ethanone (4.60 g, 19.8 mmol) in acetonitrile (39.6 mL) was added tetrabutylammoniumtribromide (TBABr3, 10.5 g, 21.8 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-(cyclopentyloxy)-2,6-dimethylphenyl)ethanone (6.2 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-3ee9a038edc043b4ad53cbe6b33ee3e3
Source noteuspto-grants-2015_04