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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369931Generated: October 30, 2026

Hydrochloric Acid → N-{1-[4-(3,4-dichlorobenzoyl)-piperidin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamide

https://huagongshe.com/reaction/369931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-(1-{4-[2-(3,4-dichlorophenyl)-[1,3]dioxolan-2-yl]piperidin-1-yl-methyl}-2-methylpropyl)-4-methylbenzamideHCID 23283153—
SolventAcetonitrileHCID 6342—
ProductN-{1-[4-(3,4-dichlorobenzoyl)-piperidin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamideHCID 9912127—

Reaction Steps

A mixture of N-(1-{4-[2-(3,4-dichlorophenyl)-[1,3]dioxolan-2-yl]piperidin-1-yl-methyl}-2-methylpropyl)-4-methylbenzamide (0.4 g, 0.791 mmol), aqueous HCl (10 mL, 6 N), and acetonitrile (10 mL) was refluxed for 2 h. After concentrating the reaction mixture, the residue was stirred with ethyl acetate and water. Sodium hydroxide solution (6 N) was added until the aqueous layer was pH 8. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organics were dried over magnesium sulfate and concentrated to give N-{1-[4-(3,4-dichlorobenzoyl)-piperidin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamide which was converted to the hydrochloride salt by adding 2 molar excess ethereal HCl (1 M) to an ether solution of the free base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140344
Source datasetuspto-grants-2000_10
ORD IDord-ccfe8d7218344c2d86889fa49f3bc49f
Source noteuspto-grants-2000_10