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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485897Generated: October 30, 2026

Hydrochloric Acid → [(2-Acetyl-6,7-dichlorobenzo[b]thien-5-yl)oxy]acetic acid

https://huagongshe.com/reaction/485897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl[(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetateHCID 53636860—
SolventEthanolHCID 702—
Product[(2-Acetyl-6,7-dichlorobenzo[b]thien-5-yl)oxy]acetic acidHCID 1329004146.9%

Reaction Steps

To 5.1 g of ethyl [(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetate in 200 ml of 95% ethanol is added 150 ml of a 6N sodium hydroxide solution and the mixture is refluxed at 100° for 45 mins. The solvent is removed in vacuo to give a white slurry to which is added 250 ml of a 6N hydrochloric acid and 200 ml ethyl ether. The mixture is stirred for 2 hrs, filtered and the filter cake is distributed between 6N hydrochloric acid and ethyl ether. The organic layers are separated and the aqueous layers are extracted with ethyl ether. The combined organic extracts are washed, dried over anhydrous magnesium sulfate, filtered and the solvent is evaporated to give a solid. Recrystallization from acetone-hexane gives 2.2 g of [(2-acetyl-6,7-dichlorobenzo[b]thien-5-yl)oxy]acetic acid, mp 203°-205°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537976
Source datasetuspto-grants-1985_08
ORD IDord-e63c362cc3534ae7ab947e553548172f
Source noteuspto-grants-1985_08