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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903491Generated: November 3, 2026

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

https://huagongshe.com/reaction/1903491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantt-Butyl [[6,7-dichloro-2-(1-hydroxy-1-methylethyl)benzo[b]thien-5-yl]oxy]acetateHCID 13290043—
SolventEthanolHCID 702—
Product[(6,7-Dichloro-2-(1-hydroxy-1-methylethyl)benzo[b]thien-5-yl]oxy]acetic acidHCID 1329004493.4%

Reaction Steps

To 8.5 g of t-butyl[ [6,7-dichloro-2-(1-hydroxy-1-methylethyl)benzo[b]thien-5-yl]oxy]acetate in 200 ml of ethanol is added 150 ml of a 6 N sodium hydroxide solution and the mixture is refluxed at 100° for 30 mins. The cooled mixture is concentrated in vacuo 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 and the ether extracts are washed, dried over anhydrous magnesium sulfate, filtered and the solvent is removed. Recrystallization of the residue from acetone and pentane gives 6.8 g of [[6,7-dichloro-2-(1-hydroxy-1-methylethyl)benzo[b]thien-5-yl]oxy]acetic acid, mp 194°-196°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436748
Source datasetuspto-grants-1984_03
ORD IDord-5293e74031664b6a8c8c8b51cfb9c6dc
Source noteuspto-grants-1984_03