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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57970082HCID 57970082—
SolventChloroformHCID 6212—
SolventDiisopropyl EtherHCID 7914—
Product6-Chloro-4-methoxyquinolin-2-OLHCID 6744339167.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044068B2
Source datasetuspto-grants-2011_10
ORD IDord-03bb7e95af7f48678a04bf7a3e91b447
Source noteuspto-grants-2011_10