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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429157Generated: October 29, 2026

Hydrochloric Acid → 3-(4-Carboxybenzyloxy)benzamide

https://huagongshe.com/reaction/429157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-Carboxymethylbenzyloxy)benzamideHCID 18354608—
Product3-(4-Carboxybenzyloxy)benzamideHCID 18354625—

Reaction Conditions

Temperature40 °C

Reaction Steps

To 3-(4-carboxymethylbenzyloxy)benzamide (Compound NU1041) (0.03 g; 0.1 mmol) was added methanol (3 ml) and aqueous sodium hydroxide (1M; 3 ml). This was warmed to 40° C., and the reaction monitored. Upon the disappearance of the starting material the solution was acidified (aqueous HCl dropwise), and extracted into ethyl acetate (3×30 ml). The organics were pooled, dried over magnesium sulphate, and the solvent removed under reduced pressure. This yielded a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316455B1
Source datasetuspto-grants-2001_11
ORD IDord-6b6adfc63820457791b75046f3fee7cb
Source noteuspto-grants-2001_11