HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604561Generated: October 26, 2026
Water → 8-[2,6-Dichloro-3-(methoxymethoxy)benzyloxy]-2-methylquinoline
https://huagongshe.com/reaction/1604561
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methyl-8-hydroxyquinoline | HCID 13224 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Dichloro-1-methylsulfonyloxymethyl-3-(methoxymethoxy)benzene | HCID 19603230 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-[2,6-Dichloro-3-(methoxymethoxy)benzyloxy]-2-methylquinoline | HCID 19603309 | — |
Reaction Steps
A solution of 8-hydroxy-2-methylquinoline (737 mg) in dimethylformamide was dropwise added to a solution of sodium hydride (60% in oil, 185 mg) in dimethylformamide under ice-bath cooling, and the mixture was stirred for 1 hour at the same temperature. To the mixture was added 2,6-dichloro-1-methylsulfonyloxymethyl-3-(methoxymethoxy)benzene (1.46 g) under ice-bath cooling, and the mixture was stirred for 1 hour at the same temperature. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by silica gel column chromatography (ethyl acetate-n-hexane) to give 8-[2,6-dichloro-3-(methoxymethoxy)-benzyloxy]-2-methylquinoline as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994368 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-cfa6cab194ea48ba92f5f2133bb9b483 |
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| Source note | uspto-grants-1999_11 |
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