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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417049Generated: October 29, 2026

Hydrochloric Acid → 4-[3-[6-(3-Benzo[1,3]dioxol-5-yl-5-isobutyryl-phenoxy)-hexyl]-2-(2-carboxy-ethyl)-phenoxy]-butyric acid

https://huagongshe.com/reaction/417049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-[3-[6-(3-Benzo[1,3]dioxol-5-yl-5-isobutyryl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl esterHCID 59496828—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-[3-[6-(3-Benzo[1,3]dioxol-5-yl-5-isobutyryl-phenoxy)-hexyl]-2-(2-carboxy-ethyl)-phenoxy]-butyric acidHCID 4692916829%

Reaction Steps

To a solution of 4-[3-[6-(3-benzo[1,3]dioxol-5-yl-5-isobutyryl-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester (191 mg) in ethanol (2 mL) was added 10 M NaOH (566 μL) and the resulting mixture was stirred at room temperature for 5 h. Then the reaction mixture was diluted with water, acidified with 3 N HCl and extracted into ethyl acetate. The organic extract was washed with brine, dried over anhydrous sodium sulfate, concentrated under reduced pressure and purified on a reverse-phase HPLC to yield 50 mg of the title compound (29% yield). HRMS calcd for C36H42O9 [M+Na]+ 641.2721, observed 641.2720.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088936B2
Source datasetuspto-grants-2012_01
ORD IDord-674b5e7dcbb34449a19b6eb9be18df62
Source noteuspto-grants-2012_01