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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903512Generated: October 30, 2026

Sodium Hydroxide → [(6,7-Dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetic acid

https://huagongshe.com/reaction/1903512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl [(6,7-dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetateHCID 13290073—
SolventEthanolHCID 702—
Product[(6,7-Dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetic acidHCID 1329007477.5%

Reaction Steps

To 16 g of ethyl[ (6,7-dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetate in 300 ml 95% ethanol is added 300 ml of a 6 N sodium hydroxide and the mixture is refluxed at 100° for 30 mins. The cooled mixture is concentrated to a white slurry which is diluted with 200 ml of ice-water and 200 ml of ethyl ether. With stirring and efficient cooling, the mixture is acidified with 6 N hydrochloric acid. The acidic mixture is extracted with ethyl ether. The ether extracts are washed, dried over anhydrous magnesium sulfate, filtered and the solvent is removed. Recrystallization of the crude product from acetone and hexane gives 11.4 g of [(6,7-dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetic acid, mp 173°-175°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436748
Source datasetuspto-grants-1984_03
ORD IDord-5d99eb0aa40d4119bde45a1892b85549
Source noteuspto-grants-1984_03