HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666659Generated: November 2, 2026
HCID 57970082, compound → 6-Chloro-4-methoxyquinolin-2-OL
https://huagongshe.com/reaction/1666659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57970082 | HCID 57970082 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 6-Chloro-4-methoxyquinolin-2-OL | HCID 67443391 | 67.4% |
Reaction Steps
Methyl 5-chloro-2-(2-(triphenyl-λ5-phosphanyliden)-acetylamino)benzoate (3.8 g) was heated at 180° C. for 1 h. The reactant was suspended in chloroform and diisopropyl ether. Solids were collected by filtration and dried to obtain 6-chloro-4-methoxyquinoline-2(1H)-one (1.1 g). (3) A mixture of 6-chloro-4-methoxyquinoline-2(1H)-one (1.1 g), N,N-dimethylaniline (1 mL), and phosphorus oxychloride (4 mL) was stirred at 80° C. to 90° C. for 10 h. The reaction solution was added dropwise to ice water and extracted with chloroform. The organic layer was dried with anhydrous magnesium sulfate, followed by addition of silica gel. The desiccant and silica gel were removed by filtration, and the filtrate was concentrated under reduced pressure to obtain 2,6-dichloro-4-methoxyquinoline (1.2 g) as pale yellow crystals.
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-03bb7e95af7f48678a04bf7a3e91b447 |
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| Source note | uspto-grants-2011_10 |
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