HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602158Generated: October 26, 2026
Potassium Carbonate → Methyl 2-[3-(tert-butoxycarbonylamino)piperidin-1-yl]benzoate
https://huagongshe.com/reaction/602158
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoic acid, 2-fluoro-, methyl ester | HCID 67854 | — |
| Reactant | 3-(Boc-amino)piperidine | HCID 4233041 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-[3-(tert-butoxycarbonylamino)piperidin-1-yl]benzoate | HCID 58992635 | 20% |
Reaction Steps
3-(tert-Butoxycarbonylamino)piperidine (7.07 g, 35.3 mmol) was dissolved in N,N-dimethylformamide (120 mL). To this solution, potassium carbonate (9.80 g, 70.9 mmol) and methyl 2-fluorobenzoate (5.0 mL, 39.2 mmol) were added and the mixture was stirred at 130° C. for 8 hours. Subsequently, the mixture was allowed to cool, diluted with ethyl acetate, and washed sequentially with water and brine. The washed product was dried over sodium sulfate and the solvent was evaporated. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=10:1->5:1) gave 2.34 g (20%) of the desired compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902367B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-9dc8db3ce1484354a405ca619454793f |
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| Source note | uspto-grants-2011_03 |
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