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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454478Generated: October 30, 2026

Sodium Hydroxide → 2-(Benzyloxy)-3-(pyridin-3-yl)benzoic acid

https://huagongshe.com/reaction/454478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl 2-(benzyloxy)-3-(pyridin-3-yl)benzoateHCID 66990338—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product2-(Benzyloxy)-3-(pyridin-3-yl)benzoic acidHCID 6699004366.6%

Reaction Steps

A 2 mol/L aqueous solution of sodium hydroxide (1.3 mL) was added to a solution mixture of the obtained benzyl 2-(benzyloxy)-3-(pyridin-3-yl)benzoate (0.35 g) in dioxane (3.5 mL) and methanol (3.5 mL), followed by stirring at room temperature for 1 hour. A 2 mol/L aqueous solution of sodium hydroxide (1.3 mL) was added to the reaction mixture, followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and water was added to the residue. After adjusting the pH to 4.5 with 6 mol/L hydrochloric acid, ethyl acetate was added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the obtained residue, and the solid substance was collected by filtration to obtain 0.18 g of 2-(benzyloxy)-3-(pyridin-3-yl)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-5487df18728b4d889ab64ad5fef46ef0
Source noteuspto-grants-2013_07