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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantm-Anisoyl chlorideHCID 74374—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTriethylamineHCID 8471—
Product3-methoxy-N-piperidin-4-ylbenzamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461182B2
Source datasetuspto-grants-2013_06
ORD IDord-40d63a453cef4425ab26bf658c9c6c4f
Source noteuspto-grants-2013_06