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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178882Generated: October 27, 2026

Trimethylbenzylammonium Dichloroiodate → 2-Chloro-1-(4,6-dichloro-1,5-naphthyridin-3-yl)ethanone

https://huagongshe.com/reaction/2178882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylbenzylammonium DichloroiodateHCID 56924451—
Reactant1-(4,6-Dichloro-1,5-naphthyridin-3-yl)ethan-1-oneHCID 89704977—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-1-(4,6-dichloro-1,5-naphthyridin-3-yl)ethanoneHCID 8970547733.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1-(4,6-dichloro-1,5-naphthyridin-3-yl)ethanone (3.0 g, 12 mmol) in THF (120 mL) was added benzyltrimethylammonium dichloroiodate (4.3 g, 12 mmol) and the reaction mixture was stirred at 70° C. for 5 h. The reaction mixture was cooled, diluted with satd. aq. sodium bicarbonate and extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated. The residue was purified by column chromatography (silica, dichloromethane/ethyl acetate) to afford the desired product (1.1 g, 32%) as an off-white solid. ESI MS m/z 275 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067937B2
Source datasetuspto-grants-2015_06
ORD IDord-b8f727e5c2c6414096f99dedcd9b69dd
Source noteuspto-grants-2015_06