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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 1-(2,4,6-Trichlorophenyl)-2-propanone | HCID 58443663 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2,4,6-Trichlorophenyl)-2-propanone O-methyloxime | HCID 76787515 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258169B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-fdfa6c25699b4fa8a85eb7bd18158c55 |
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| Source note | uspto-grants-2012_09 |
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