HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335229Generated: October 26, 2026
1-acetyl-N-methoxy-N-methylpiperidine-4-carboxamide → 1,4-Diacetylpiperidine
https://huagongshe.com/reaction/335229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-acetyl-N-methoxy-N-methylpiperidine-4-carboxamide | HCID 18713548 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,4-Diacetylpiperidine | HCID 2777250 | 82.2% |
Reaction Steps
1-Acetyl-N-methoxy-N-methylpiperidine-4-carboxamide (59.10 g, 276 mmol) was dissolved in THF (800 mL) and cooled to 0° C. Methylmagnesium bromide (110.3 mL, 331 mmol) (3.0M in diethyl ether) was added slowly and the resulting white slurry was agitated for 1 hour. The reaction was quenched with 300 mL of 2M HCl and the solvent was evaporated. The resulting aqueous slurry was filtered and the solids were washed with water and small amount of ether to provide the title compound (38.4 g, 82.2% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883828B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-89e4189071c443b4bdd0d4fe1bcdbe85 |
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| Source note | uspto-grants-2014_11 |
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