HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46580Generated: October 27, 2026
Triethylamine → 3-(2,6-dimethylphenylamino)-2-butanone O-methyloxime
https://huagongshe.com/reaction/46580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 3-(2,6-Dimethylphenylamino)-2-butanone | HCID 12491475 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2,6-dimethylphenylamino)-2-butanone O-methyloxime | HCID 54149925 | — |
Reaction Steps
A sample of 50.5 g triethylamine was added dropwise to a solution of 50.1 g (0.6 mol) methoxyamine hydrochloride in 75 ml dichloromethane at 9°-20° C. To the resulting solution was added about one-half of a 95.6-g (0.5-mol) sample of 3-(2,6-dimethylphenylamino)-2-butanone. The reaction temperature rose from 16° C. to 30° C. The reaction mixture was cooled in an ice bath, and the remaining 3-(2,6-dimethylphenylamino)-2-butanone was added dropwise. The reaction mixture was then stirred about 18 hours at about 20° C., washed with 50 ml of water and evaporated under reduced pressure to give 100.3 g of 3-(2,6-dimethylphenylamino)-2-butanone O-methyloxime, as an oil. The nuclear magnetic resonance spectrum showed a sharp 3-proton singlet (--OCH3) at 3.9 ppm (relative to tetramethylsilane) and a sharp 6-proton singlet (2,6-dimethyl groups) at 2.2 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04174210 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-8c9f8b193ed54ce892b4c0d2477e7e72 |
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| Source note | uspto-grants-1979_11 |
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