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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370951Generated: October 29, 2026

HCID 13290017, compound → HCID 13290018, compound

https://huagongshe.com/reaction/370951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13290017HCID 13290017—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductHCID 13290018HCID 1329001889%

Reaction Steps

A mixture of 1.5 g ethyl[(6,7-dichloro-3-methyl-2-phenylbenzo[b]thien-5-yl)oxy]acetate in 50 ml of 95% ethanol and 50 ml of 15% aqueous sodium hydroxide is stirred under reflux for 1 hour. The mixture is concentrated under vacuum to dryness. The residue is triturated with water, cooled to 0° and acidified with conc hydrochloric acid. The solid product is extracted exhaustively with a mixture of ethyl ether-ethyl acetate (1:1) and the ether extracts are washed and dried over anhydrous magnesium sulfate. Removal of the solvents under reduced pressure leaves a tan-colored residue which is recrystallized from acetone to give 1.24 g of [(6,7-dichloro-3-methyl-2-phenylbenzo[b]thien-5-yl)oxy]acetic acid as shiny platelets, mp 232°-233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528399
Source datasetuspto-grants-1985_07
ORD IDord-41636959bdef4fb7b50fb6ea46b7fbd3
Source noteuspto-grants-1985_07