HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584591Generated: October 29, 2026
Pyridine → 4-Dimethylaminocyclohexanone oxime
https://huagongshe.com/reaction/1584591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4-(Dimethylamino)cyclohexan-1-one--hydrogen chloride (1/1) | HCID 12717448 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Dimethylaminocyclohexanone oxime | HCID 10877370 | 67.2% |
Reaction Steps
A mixture of 1.78 gm (10 mMol) of 4-dimethylaminocyclohexanone hydrochloride and 0.70 gm (10 mMol) of hydroxylamine hydrochloride in 25 mL ethanol was treated with 3 mL pyridine and then heated at reflux for 30 minutes. The reaction mixture was then cooled to room temperature and stored at 4° C. for 18 hours. The resulting crystalline solid was collected and washed with cold ethanol. The solid was then dissolved in water and the aqueous solution made basic by the addition of potassium carbonate. The aqueous phase was then extracted with dichloromethane which contained a small amount of isopropanol. The organic extracts were combined, dried over sodium sulfate and concentrated under reduced pressure to provide a crystalline solid. This solid was recrystallized from ethanol to provide 1.05 gm (67%) of the desired oxime.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932739 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-5c79a3cc98ca4dd6a9ea007ac4ffa243 |
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| Source note | uspto-grants-1999_08 |
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