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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423518Generated: November 2, 2026

1-(5-Bromo-2-nitrophenyl)ethan-1-ol → 1-(5-Bromo-2-nitrophenyl)ethanone

https://huagongshe.com/reaction/2423518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Bromo-2-nitrophenyl)ethan-1-olHCID 45073390—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product1-(5-Bromo-2-nitrophenyl)ethanoneHCID 1222415777%

Reaction Steps

Jones Reagent (2.67 M, 2.54 mL, 6.79 mmol) was added dropwise to 1-(5-bromo-2-nitrophenyl)-ethanol (1.67 g, 6.79 mmol) in acetone (34 mL) at 0° C., then the reaction mixture was stirred for 10 minutes. Any excess Jones reagent was quenched by the addition of iso-propanol, then the reaction mixture was neutralized with saturated sodium bicarbonate, and the acetone was removed by evaporation. Water was added and the solution was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, then filtered and concentrated. The residue was purified by silica gel chromatography eluting with 1:9 ethyl acetate:hexanes to give 1.27 g (77%) of 1-(5-bromo-2-nitrophenyl)-ethanone as a solid. 1H NMR (400 MHz, d6-DMSO): δ 8.05 (d, J=5 Hz, 1H), 8.04 (s, 1H), 7.96 (dd, J=9, 2 Hz, 1H), 2.57 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960552B2
Source datasetuspto-grants-2011_06
ORD IDord-65099191847e4dec8488c819bda6cb39
Source noteuspto-grants-2011_06