Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454464Generated: October 27, 2026

Hydrochloric Acid → 2-(Benzyloxy)-4-(pyridin-3-yl)benzoic acid

https://huagongshe.com/reaction/454464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl 2-(benzyloxy)-4-(pyridin-3-yl)benzoateHCID 66990951—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2-(Benzyloxy)-4-(pyridin-3-yl)benzoic acidHCID 6698997874%

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)-4-(pyridin-3-yl)benzoate (0.35 g) in dioxane (1.8 mL) and methanol (1.8 mL), followed by stirring at room temperature for 1 hour. Water was added to the reaction mixture. 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 0.20 g of 2-(benzyloxy)-4-(pyridin-3-yl)benzoic acid as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-cb8f4464a53e4d48a87cd1413f40c64b
Source noteuspto-grants-2013_07