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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485849Generated: October 26, 2026

Ethyl bromoacetate → Ethyl[(6,7-dichlorobenzo[b]thien-5-yl)oxy]acetate

https://huagongshe.com/reaction/485849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant6,7-Dichloro-1-benzothiophene-5-olHCID 13289997—
SolventDimethylformamideHCID 6228—
ProductEthyl[(6,7-dichlorobenzo[b]thien-5-yl)oxy]acetateHCID 1328999963.8%

Reaction Steps

A mixture of 3.6 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene, 3.0 g of ethyl bromoacetate, 1.5 g of potassium carbonate and 40 ml of anhydrous dimethylformamide is stirred at 70°-80° for 16 hours. The cooled mixture is diluted with ice-water (200 g) and the solid collected by filtration. Recrystallization of the crude product from acetone-hexane gives 3.2 g of ethyl [(6,7-dichlorobenzo[b]thien-5-yl)oxy]acetate as yellowish needles, mp 92°-93°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537976
Source datasetuspto-grants-1985_08
ORD IDord-1930dce74430403d89f3c7b8d41e4795
Source noteuspto-grants-1985_08