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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416987Generated: October 30, 2026

Sodium Hydroxide → HCID 46928679, compound

https://huagongshe.com/reaction/416987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59496796HCID 59496796—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46928679HCID 4692867995%

Reaction Steps

To a solution of the 4-[3-[6-(3-benzo[1,3]dioxol-5-yl-5-ethoxy-phenoxy)-hexyl]-2-(2-ethoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester (152 mg, 0.23 mmol) in THF (5 mL) and ethanol (5 mL) was added aqueous 1.0 N sodium hydroxide (5 mL) at room temperature. The resulting suspension was stirred for 5 h at room temperature at which time TLC analysis of the mixture indicated the absence of starting material. Then, the reaction mixture was concentrated and the residue was diluted with water (20 mL) and extracted with diethyl ether (30 mL) to remove any neutral impurities. The aqueous layer was acidified with 1.0 N hydrochloric acid and the precipitated white organic compound was extracted into ethyl acetate (2×30 mL). The combined ethyl acetate extracts were washed with brine solution (50 mL) and the organic layers were dried over anhydrous magnesium sulfate. Filtration of the drying agent and removal of the solvent afforded 4-[3-[6-(3-benzo[1,3]dioxol-5-yl-5-ethoxy-phenoxy)-hexyl]-2-(2-carboxy-ethyl)-phenoxy]-butyric acid (129 mg, 95%) as a off-white waxy solid: ES(+)-HRMS m/e calcd for C34H40O9 (M+H)+ 593.2745. found 593.2744.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088936B2
Source datasetuspto-grants-2012_01
ORD IDord-0f8661365e5c4c098e510c9f746cb53e
Source noteuspto-grants-2012_01