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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652685Generated: October 26, 2026

Dimethylformamide → Ethyl [(6,7-dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetate

https://huagongshe.com/reaction/652685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanolHCID 13477654—
SolventMethyl Ethyl KetoneHCID 6569—
ProductEthyl [(6,7-dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetateHCID 1329007386.4%

Reaction Steps

To a solution of 17 g of 6,7-dichloro-5-hydroxy-α-methylbenzo[b]thiophene-2-methanol in 250 ml of 2-butanone is added a solution of 11.8 g of ethyl bromoacetate in 50 ml 2-butanone and the mixture is heated at 95°. To the mixture is added 12 g of potassium carbonate and 5.3 ml of dimethylformamide and the reaction mixture is refluxed at 100° for 21/2 hrs. The cooled mixture is filtered and 100 ml of water is added. The aqueous phase is extracted two times with ethyl ether. The ether extracts are washed, dried over anhydrous magnesium sulfate, filtered and concentrated to give a solid. Recrystallization from acetone and hexane gives 19.5 g of ethyl[(6,7-dichloro-2-(1-hydroxyethyl)benzo[b]thien-5-yl)oxy]acetate, mp 101°-103°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04672138
Source datasetuspto-grants-1987_06
ORD IDord-8546328d698b460693c1df5086df3736
Source noteuspto-grants-1987_06