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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217710Generated: October 30, 2026

Water → 2-Bromo-1-[3-methoxy-5-(pentafluorosulfanyl)phenyl]ethanone

https://huagongshe.com/reaction/217710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant1-[3-Methoxy-5-(pentafluorosulfanyl)phenyl]ethanoneHCID 44183118—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-[3-methoxy-5-(pentafluorosulfanyl)phenyl]ethanoneHCID 58136835105.4%

Reaction Steps

1-[3-Methoxy-5-(pentafluorosulfanyl)phenyl]ethanone (O2.007; 1.63 g) was dissolved in THF (150 ml), and phenyltrimethylammonium tribromide (2.2 g) was added at RT while stirring. After stirring at RT for 2 h, the mixture was admixed with water, neutralized with sodium hydrogencarbonate solution and extracted three times with EA. The alkaline water phase was extracted 3× with EA. The combined organic phases were dried over magnesium sulfate and, after the desiccant had been filtered off, dried under reduced pressure. The residue was purified by means of preparative HPLC (met. A). The product fractions, each of them clean, were combined, freed of the acetonitrile under reduced pressure, neutralized with sodium hydrogencarbonate and extracted three times with EA. The combined organic phases were dried over magnesium sulfate and, after the desiccant had been filtered off, dried under reduced pressure. 1.27 g of the title compound were isolated. LC-MS rt: 1.65 min [M+H]+: 354.9 (met. b)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-6b6e39ad3d7644df9e2a18be0e1447bd
Source noteuspto-grants-2012_06