HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887378Generated: October 30, 2026
Ethyl Acetate → 1-(1-Benzylpiperidin-4-yl)ethanone
https://huagongshe.com/reaction/887378
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide | HCID 21193030 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(1-Benzylpiperidin-4-yl)ethanone | HCID 910923 | — |
Reaction Steps
To a stirred solution of 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide (11.5 g, 44 mmol) in diethyl ether (150 mL) at 0° C. was added methyl magnesium bromide (15.7 g, 132 mmol), drop-wise over 10 min. The resulting mixture was stirred at 25-30° C. for 2 h. After completion of the reaction, the mixture was treated with EtOAc and saturated NH4Cl solution. The separated organic layer was washed with brine and dried over anhydrous sodium sulfate and concentrated under vacuum to afford 1-(1-benzylpiperidin-4-yl)ethanone product. [M+1]=218.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247418B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-f2d4fe5c3c7f4c04977529d2f4e1cfcc |
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| Source note | uspto-grants-2012_08 |
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