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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381257Generated: November 2, 2026

Triethylamine → 1-(2,4,6-Trichlorophenyl)-2-propanone O-methyloxime

https://huagongshe.com/reaction/2381257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant1-(2,4,6-Trichlorophenyl)-2-propanoneHCID 58443663—
SolventMethanolHCID 887—
Product1-(2,4,6-Trichlorophenyl)-2-propanone O-methyloximeHCID 7678751576%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of O-methyl-hydroxylamine hydrochloride (0.79 g, 9.4 mmol) in methanol (20 ml) was treated with triethylamine (1.32 ml, 9.4 mmol) followed by 1-(2,4,6-trichlorophenyl)-propan-2-one (1.5 g, 6.31 mmole). The resulting mixture was stirred at 60° C. for 3 hours. The reaction mixture was quenched with water and methanol was evaporated off. The resulting aqueous medium was extracted with ethylacetate (3×50 ml). The combined organic layers were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated under reduced pressure (100 mbar; 45° C.). The resulting crude mass was purified by column chromatography using 60-120μ mesh silica gel and product collected at 2% ethyl acetate in hexane as elution system to give 1-(2,4,6-Trichloro-phenyl)-propan-2-one O-methyl-oxime (1.2 g, 76%), which was taken up for further reduction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258169B2
Source datasetuspto-grants-2012_09
ORD IDord-fdfa6c25699b4fa8a85eb7bd18158c55
Source noteuspto-grants-2012_09