Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600795Generated: October 29, 2026

Water → 1-bromo-3-phenyl-2-propanone

https://huagongshe.com/reaction/600795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEpibromohydrinHCID 18430—
ReactantJones' reagentHCID 131709961—
ReactantHCID 178418255HCID 178418255—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
Product1-bromo-3-phenyl-2-propanoneHCID 1146992775.1%

Reaction Steps

To a suspension of CuBr (0.143 g, 0.997 mmol) in 25 mL dry ether was slowly added 1M phenylmagnesium bromide (10 mL, 10 mmol). Epibromohydrin (0.87 mL, 10.5 mmol) was then added dropwise. The reaction mixture was allowed to stir at −78° C. to room temperature overnight, poured into H2O and extracted with ether. The extracts were washed with H2O and brine, dried over Na2SO4, filtered and evaporated in vacuo. The crude alcohol thus obtained was dissolved in acetone (400 mL) and chilled in ice, and to this solution was added dropwise 6 mL of Jones reagent (prepared by dissolution of 2.67 g CrO3 in 2.5 mL H2SO4, followed by dilution with H2O to 10 mL). The reaction mixture was stirred at 0° C. for 15 min and was then evaporated in vacuo. The residue was taken up in ethyl acetate, washed repeatedly with water and once with brine, dried over Na2SO4, filtered and evaporated to afford the ketone product as a brown oil (1.6 g, 75%). 1H NMR (DMSO-d6) δ 7.17-7.35 (m, 5H), 4.45 (s, 2H), 3.94 (s, 2H); MS (DCI+) m/z 230 (M+NH4+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902236B2
Source datasetuspto-grants-2011_03
ORD IDord-2668dc585eb14e0fac05b0d11da0f3a8
Source noteuspto-grants-2011_03