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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823102Generated: November 1, 2026

Sodium Hydroxide → Benzoic Acid

https://huagongshe.com/reaction/1823102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69056508HCID 69056508—
SolventEthanolHCID 702—
ProductBenzoic AcidHCID 243—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of ethyl 4′-[2-[(tert-butoxycarbonyl)-[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]-2-methoxy-1,1′-biphenyl-4-carboxylate (220 mg) in ethanol (2.0 ml) was added 1N aqueous sodium hydroxide solution (1.2 ml), and the mixture was stirred at 40° C. for 3 hours. The solvent was removed by evaporation, and the aqueous solution was acidified with 1N hydrochloric acid and extracted with ethyl acetate (30 ml×2). The combined organic layers were washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure to give a benzoic acid product. To a solution of the product in tetrahydrofuran (1.5 ml) was added 4N hydrochloride in dioxane (1.0 ml), and the mixture was stirred at room temperature for 12 hours. The resultant solid was collected by filtration and dried to give 4′-[2-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]-ethyl]-2-methoxy-1,1′-biphenyl-4-carboxylic acid hydrochloride (83 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037938B2
Source datasetuspto-grants-2006_05
ORD IDord-2830be2775f14bd488b23d7b12ca0a92
Source noteuspto-grants-2006_05