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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194556Generated: November 1, 2026

5'-Bromo-2'-hydroxyacetophenone → 1-(5-Bromo-2-hydroxyphenyl)ethanone oxime

https://huagongshe.com/reaction/2194556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantPotassium AcetateHCID 517044—
SolventEthanolHCID 702—
Product1-(5-Bromo-2-hydroxyphenyl)ethanone oximeHCID 13553801498.2%

Reaction Steps

To a solution of 1-(5-bromo-2-hydroxyphenyl)ethanone (2.0 g, 9.30 mmol) in ethanol (20 mL) were added hydroxylamine hydrochloride (0.7 g, 10.2 mmol) and potassium acetate (1.0 g, 10.2 mmol). The mixture was stirred at reflux temperature for 16 h. After this time, the mixture was cooled, concentrated and the residue was diluted with CH2Cl2 (25 mL) and washed with H2O (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford title compound (11) (2.1 g, 95%) as a white solid. 1H NMR (CDCl3, 400 MHz) δ 7.40 (s, 1H), 7.20 (dd, J=8.8, 2.0 Hz, 1H), 6.72 (d, J=8.8 Hz, 1H), 2.50 (bs, 1H), 2.20 (s, 3H); MS (ESI, M+H+) C8H9BrNO2, calcd. 230.0. found 230.0, 232.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334292B1
Source datasetuspto-grants-2012_12
ORD IDord-fa8953a7f9bc40d7af1ec9b475f5136a
Source noteuspto-grants-2012_12