HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256278Generated: November 1, 2026
Hydrochloric Acid → 3-methoxy-N-piperidin-4-ylbenzamide
https://huagongshe.com/reaction/1256278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | m-Anisoyl chloride | HCID 74374 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-methoxy-N-piperidin-4-ylbenzamide | HCID 1445157 | — |
Reaction Steps
Step R1-4: To a solution of tert-butyl 4-aminopiperidine-1-carboxylate (150 g) and Et3N (209 mL) in IPA (1.0 L) was added 3-methoxybenzoyl chloride (102 mL) over 40 minutes under ice cooling. The mixture was stirred at room temperature for 2 hours. After cooling to 0° C., 12 M aqueous HCl (0.5 L) was added to the mixture over 30 minutes and the mixture was stirred at 50° C. for 1 hour. After cooling to 0° C., 12 M aqueous NaOH (0.5 L) and water (0.4 L) were added over 40 minutes to the reaction mixture. The organic layer was separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and concentrated to obtain 3-methoxy-N-(piperidin-4-yl)benzamide as a light brown solid (160 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461182B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-40d63a453cef4425ab26bf658c9c6c4f |
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| Source note | uspto-grants-2013_06 |
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