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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454576Generated: October 29, 2026

Hydrochloric Acid → 2-(2-Hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoic acid

https://huagongshe.com/reaction/454576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoateHCID 58508867—
SolventMethanolHCID 887—
Product2-(2-Hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoic acidHCID 5850844833.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 2.0 mol/L aqueous solution of sodium hydroxide (0.33 mL) was added to a methanol (2.0 mL) suspension of the obtained methyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate (0.058 g), followed by stirring at 60° C. for 9 hours and 20 minutes. The reaction mixture was cooled to room temperature, and 6 mol/L hydrochloric acid (0.11 mL) was added thereto. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 95-85% chloroform/methanol] to obtain 0.019 g of 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-d817427eb2b5422ca232ca8dacbf2642
Source noteuspto-grants-2013_07