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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454724Generated: October 30, 2026

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

https://huagongshe.com/reaction/454724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-(2-hydroxy-5-(1-isopropylpiperidin-4-yl)benzamido)-4-phenylbenzoateHCID 58508803—
SolventWaterHCID 962—
Product2-(2-Hydroxy-5-(1-isopropylpiperidin-4-yl)benzamido)-4-phenylbenzoic acidHCID 5850861474.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

A 2.0 mol/L aqueous solution of sodium hydroxide (0.27 mL) was added to a 2-propanol (1.5 mL) suspension of the obtained methyl 2-(2-hydroxy-5-(1-isopropylpiperidin-4-yl)benzamido)-4-phenylbenzoate (0.086 g), followed by stirring at 50° C. for 1 hour. A 2.0 mol/L aqueous solution of sodium hydroxide (0.091 mL) was added to the reaction mixture, followed by stirring at 50° C. for 30 minutes. The reaction mixture was cooled to room temperature, and water was added thereto. After adjusting the pH to 6.0 with 1.0 mol/L hydrochloric acid, the solid substance was collected by filtration to obtain 0.062 g of 2-(2-hydroxy-5-(1-isopropylpiperidin-4-yl)benzamido)-4-phenylbenzoic acid as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-d7b14c02e40d462aa361be3debb93299
Source noteuspto-grants-2013_07