Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652667Generated: October 30, 2026

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

https://huagongshe.com/reaction/652667

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 6N 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 6N 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 numberUS04672138
Source datasetuspto-grants-1987_06
ORD IDord-ff1acf4866d34469bf764a7051f31359
Source noteuspto-grants-1987_06