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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177666Generated: October 30, 2026

Acetic Acid → 6-(Benzenesulphonylmethyl)-3-ethyl-2-methoxy-benzoic acid

https://huagongshe.com/reaction/2177666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
ReactantLithium HydroxideHCID 3939—
ReactantEthyl 6-(phenylthiomethyl)-3-ethyl-2-methoxybenzoateHCID 67107436—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6-(Benzenesulphonylmethyl)-3-ethyl-2-methoxy-benzoic acidHCID 52913862—

Reaction Conditions

Temperature60 °C

Reaction Steps

Hydrogen peroxide (30% aqueous solution, 0.117 ml) was added to a solution of ethyl 6-(phenylthiomethyl)-3-ethyl-2-methoxybenzoate (Intermediate 19, 0.057 g) in acetic acid (1.7 ml) and the resultant solution was stirred and heated at 60° C. for 2 hours. After cooling, the solution was evaporated to dryness to give the crude sulphone. The residue was dissolved in a mixture of dioxane (1 ml) and water (1 ml) and lithium hydroxide (0.072 g) was added. The mixture was stirred and heated in the microwave at 160° C. for 15 minutes. After cooling, the mixture was evaporated to dryness and the residue was acidified by addition of hydrochloric acid (1M) and then immediately purified by preparative HPLC (C18) eluting with a mixture of methanol and water containing 0.1% formic acid to give 6-(benzenesulphonylmethyl)-3-ethyl-2-methoxy-benzoic acid (0.022 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-63061ef805dd4d969c641f917f417588
Source noteuspto-grants-2015_06