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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395652Generated: October 25, 2026

Bromine → Ethyl 5-bromo-6-(5-chloro-2-thienyl)-6-oxohexanoate

https://huagongshe.com/reaction/395652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
ReactantEthyl 6-(5-chloro-2-thienyl)-6-oxohexanoateHCID 18174688—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-bromo-6-(5-chloro-2-thienyl)-6-oxohexanoateHCID 18174681118.8%

Reaction Steps

Ethyl 6-(5-chloro-2-thienyl)-6-oxohexanoate (50.0 g) was dissolved in methylene chloride (150 ml), to which was added dropwise bromine (24.5 g) with stirring at room temperature. The mixture was stirred at room temperature for 1 hour, a 10% aqueous solution of sodium sulfite was then carefully added until disappearance of the red color of bromine, which was extracted with diethyl ether (200 ml×2). The organic layer was washed with a10% aqueous solution of sodium hydrogen carbonate (100 ml), dried over anhydrous magnesium sulfate, and concentrated to give ethyl 5-bromo-6-(5-chloro-2-thienyl)-6-oxohexanoate as an oil (64.4 g, >99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605629B1
Source datasetuspto-grants-2003_08
ORD IDord-fbc80386f6dc4b9d9f5ee07ddeb445f6
Source noteuspto-grants-2003_08