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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177681Generated: October 31, 2026

Ethyl Acetate → 6-(Benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoic acid

https://huagongshe.com/reaction/2177681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 6-(benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoateHCID 67108200—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6-(Benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoic acidHCID 5291317530.5%

Reaction Conditions

Temperature150 °C

Reaction Steps

Lithium hydroxide monohydrate (0.075 g) was added to a solution of methyl 6-(benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoate (Intermediate 152, 0.092 g) in dioxane (1 ml) and water (1 ml) and the resultant solution was stirred and heated in the microwave at 150° C. for 4.5 hours. Ethyl acetate and water were added and the organic layer was separated, then acidified with concentrated hydrochloric acid. The mixture was extracted with ethyl aceate, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness then azeotroped with toluene. The residue was triturated with ether and the solid was collected by filtration and dried to give 6-(benzenesulphonylmethyl)-2-ethyl-3-(furan-3-yl)benzoic acid (0.027 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-c5499c1ca6e54861a797e496ee6a37df
Source noteuspto-grants-2015_06