HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911084Generated: October 26, 2026
1-acetyl-N-methoxy-N-methylpiperidine-4-carboxamide → 1,4-Diacetylpiperidine
https://huagongshe.com/reaction/911084
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 | 82.3% |
Reaction Steps
1-Acetyl-N-methoxy-N-methylpiperidine-4-carboxamide (59.10 g, 275.8 mmol) was dissolved in tetrahydrofuran (800 ml) and cooled to 0° C. Methylmagnesium bromide (110.3 ml, 331.0 mmol) (3.0 M 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 organic solvent was evaporated. The resulting aqueous slurry was extracted three times with 20:80 isopropanol/chloroform. The resulting extracts were washed with brine and evaporated to produce the desired product (38.40 g, 82.27% yield) as amber oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022222B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-da20895bae894ced9f8f891ae58cebd5 |
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| Source note | uspto-grants-2011_09 |
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