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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843762Generated: November 3, 2026

Tetra-n-butylammonium tribromide → HCID 58442393, compound

https://huagongshe.com/reaction/1843762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium tribromideHCID 23500184—
ReactantHCID 58442529HCID 58442529—
SolventAcetonitrileHCID 6342—
ProductHCID 58442393HCID 58442393109.2%

Reaction Steps

To a solution of 1-(4-(benzo[d][1,3]dioxol-5-yloxy)-2,6-dimethylphenyl)ethanone (4.80 g, 16.9 mmol) in acetonitrile (33.8 mL) was added tetrabutylammoniumtribromide (TBABr3, 8.14 g, 16.9 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 1-(4-(benzo[d][1,3]dioxol-5-yloxy)-2,6-dimethylphenyl)-2-bromoethanone (6.70 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-0f35123529e94e0bb395a7eabba07af4
Source noteuspto-grants-2015_02