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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylbenzylammonium Dichloroiodate | HCID 56924451 | — |
| Reactant | 1-(4,6-Dichloro-1,5-naphthyridin-3-yl)ethan-1-one | HCID 89704977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-1-(4,6-dichloro-1,5-naphthyridin-3-yl)ethanone | HCID 89705477 | 33.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345709B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-d13c883052814b55a1b77a395cbc21dc |
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| Source note | uspto-grants-2016_05 |
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