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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747457Generated: October 25, 2026

Bromine → Ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoate

https://huagongshe.com/reaction/747457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
ReactantEthyl 6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174724—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174722—

Reaction Steps

Ethyl 6-(4-fluoro-1-naphthyl)-6-oxohexanoate (27.7 g) was dissolved in methylene chloride (100 ml), and bromine (14.6 g) was added dropwise with stirring at room temperature. After an hour of stirring at room temperature, a 10% aqueous solution of sodium sulfite was carefully added until disappearance of the red color of bromine, which was extracted with diethyl ether (300 ml×2). The organic layer was washed with a 10% aqueous solution of sodium hydrogen carbonate (100 ml), dried over anhydrous magnesium sulfate, and concentrated to give ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoate as an oil (34.9 g, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396848B1
Source datasetuspto-grants-2008_07
ORD IDord-f9d587e51908422b99d73dcfb3ce2c6e
Source noteuspto-grants-2008_07