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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418066Generated: October 31, 2026

Sodium Hydroxide → 4-{2-(2-Carboxy-ethyl)-3-[6-(3-iodo-5-methanesulfonyl-phenoxy)-hexyl]-phenoxy}-butyric Acid

https://huagongshe.com/reaction/418066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-{2-(2-Ethoxycarbonyl-ethyl)-3-[6-(3-iodo-5-methanesulfonyl-phenoxy)-hexyl]-phenoxy}-butyric Acid Ethyl EsterHCID 57863037—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product4-{2-(2-Carboxy-ethyl)-3-[6-(3-iodo-5-methanesulfonyl-phenoxy)-hexyl]-phenoxy}-butyric AcidHCID 5786312297.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-{2-(2-ethoxycarbonyl-ethyl)-3-[6-(3-iodo-5-methanesulfonyl-phenoxy)-hexyl]-phenoxy}-butyric acid ethyl ester (0.9 g, 1.31 mmol) in hot ethanol (40 mL) was added aqueous 1.0 N sodium hydroxide (10 mL). The resulting solution was heated to 60° C. and stirred for 4 h. Then, the reaction mixture was cooled down and diluted with EtOAc, washed with 10% HCl and brine. The combined ethyl acetate extracts were dried over anhydrous sodium sulfate, concentrated under reduced pressure to afford 805 mg (97%) of title compound as a light yellow oil. HR-ES(+) m/e calcd for C26H33O8SI (M+H)+ 633.1014, found 633.1008.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093253B2
Source datasetuspto-grants-2012_01
ORD IDord-2da7dbbdd59e4a698949883a6c510278
Source noteuspto-grants-2012_01