HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465709Generated: October 31, 2026
Tert-butyl 3-[methoxy(methyl)carbamoyl]piperidine-1-carboxylate → tert-Butyl 3-acetylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1465709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl 3-[methoxy(methyl)carbamoyl]piperidine-1-carboxylate | HCID 22248320 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 3-acetylpiperidine-1-carboxylate | HCID 25260002 | 70.4% |
Reaction Steps
Tert-butyl 3-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate (8.17 g, 30 mmol) was dissolved in THF (100 mL) and cooled to 0° C., methylmagnesium bromide (3.0 M in Et2O, 11 mL, 33 mmol) was added dropwise. The reaction mixture was warmed to room temperature and stirred overnight. After quench with saturated NH4Cl, the reaction mixture was extracted with EtOAc, dried and concentrated. The crude product was column purified with mixture of hexane and EtOAc to give tert-butyl 3-acetylpiperidine-1-carboxylate (4.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999966B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-6c45a7c41d2a49748a83d3c5b41057ae |
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| Source note | uspto-grants-2015_04 |
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