HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666697Generated: October 30, 2026
Methanol → 2-Chloro-6-methoxymethyl-4-methylquinoline
https://huagongshe.com/reaction/1666697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14991293 | HCID 14991293 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-6-methoxymethyl-4-methylquinoline | HCID 57970220 | — |
Reaction Steps
To a solution of 6-bromomethyl-2-chloro-4-methylquinoline (0.40 g) in methanol (8 mL) was added 1 M aqueous sodium hydroxide (4 mL) at room temperature, and the mixture was stirred at 70° C. for 30 min. After cooled to room temperature, the reaction solution was diluted with ethyl acetate. The organic layer was washed with saturated brine, the organic layer was dried with anhydrous magnesium sulfate, the desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1:4) to obtain 2-chloro-6-methoxymethyl-4-methylquinoline (0.31 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044068B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-bfdb44c2d3024111a1cbb87ed9e87de1 |
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| Source note | uspto-grants-2011_10 |
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