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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526161Generated: October 26, 2026

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

https://huagongshe.com/reaction/526161

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 numberUS09345709B2
Source datasetuspto-grants-2016_05
ORD IDord-d13c883052814b55a1b77a395cbc21dc
Source noteuspto-grants-2016_05