HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethylpiperidine-2,4-dione → 1-Ethyl-3-methoxymethylenepiperidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethylpiperidine-2,4-dione | HCID 13784119 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 1-Ethyl-3-methoxymethylenepiperidine-2,4-dione | HCID 54092152 | 25.1% |
Reaction Steps
Added to 8.3 g of 1-ethylpiperidine-2,4-dione were 11 g of methyl orthoformate and 20 ml of acetic anhydride. The resultant mixture was refluxed for 7 hours. After allowing the reaction mixture to cool down, excess methyl orthoformate and acetic anydride were distilled off under reduced pressure. The brown residue was distilled under reduced pressure in a Kugelroll apparatus (0.5 mmHg; bath temperature: 200°-250° C.) to obtain 2.7 g of 1-ethyl-3-methoxymethylenepiperidine-2,4-dione as crystals (yield: 25%). The crystals were recrystallized from a mixed solvent of ethyl acetate and hexane to obtain needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734418 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-31eebf9e4afb46a98abce0f961ffe098 |
| Source note | uspto-grants-1988_03 |