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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480684Generated: November 1, 2026

Tetra-n-butylammonium tribromide → HCID 58442393, compound

https://huagongshe.com/reaction/1480684

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 numberUS09409902B2
Source datasetuspto-grants-2016_08
ORD IDord-839ba236c0a645288a836cbfa204bd4c
Source noteuspto-grants-2016_08