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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715056Generated: November 1, 2026

Sodium Hydroxide → HCID 59028779, compound

https://huagongshe.com/reaction/1715056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59028778HCID 59028778—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 59028779HCID 5902877986.3%

Reaction Steps

3-[6-(3-Fluoro-benzenesulfonyl)-naphthalen-1-yl]-propionic acid ethyl ester (2.0 g) was dissolved in 25 mL ethanol, and 10 mL of 25% aqueous NaOH was added. The reaction mixture was heated to reflux for one hour, then cooled to room temperature. The ethanol was removed under reduced pressure, and the liquid residue was acidified by addition of 10% aqueous HCl. The mixture was extracted with EtOAc, and the combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure to give a crude oil. The oil was dissolved in warm toluene and insolubles were removed by filtration. The filtrate was concentrated under reduced pressure to give 1.6 g of 3-[6-(3-fluoro-benzenesulfonyl)-naphthalen-1-yl]-propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799797B2
Source datasetuspto-grants-2010_09
ORD IDord-cc53eff756fb444ca3b4cdf29e10a21a
Source noteuspto-grants-2010_09