HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555795Generated: October 26, 2026
Benzyl Bromide → 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide
https://huagongshe.com/reaction/555795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methoxy-N-methylpiperidine-4-carboxamide | HCID 22405751 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide | HCID 21193030 | — |
Reaction Steps
To the solution of N-methoxy-N-methylpiperidine-4-carboxamide (40 g, 232 mmol) in acetone (400 mL) was added benzyl bromide (42 mL, 349 mmol) and K2CO3 (64 g, 465 mmol) and the reaction mixture was stirred at 80° C. under reflux for 16 h. After completion of the reaction, the reaction mixture was filtered and acetone was removed under reduced pressure. The residue was purified by silica gel column chromatography (eluting with 50% ethyl acetate in hexane) to afford 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide product. [M+1]=263.15
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053438B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-423421afcf784d10b678fc366786b729 |
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| Source note | uspto-grants-2011_11 |
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