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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445462Generated: October 28, 2026

Water → 7-(Benzyloxy)-4-chloro-6-methoxyquinoline

https://huagongshe.com/reaction/445462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant7-Benzyloxy-6-methoxy-3H-quinazolin-4-oneHCID 135404718—
SolventDichloromethaneHCID 6344—
Product7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 2264656248%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dry DMF (8.0 ml, 103 mmol) was dissolved in dry CHCl3 (40 ml) and cooled in an ice bath. Oxalyl chloride (9.0 ml, 105 mmol) in CH2Cl2 (10 ml) was added dropwise with stirring at 0° C. When the bubbling had ceased, this solution was added slowly to an ice-cold solution of 7-benzyloxy-6-methoxy-3H-quinazolin-4-one (10.0 g, 35.4 mmol) in dry CHCl3 (60 ml) and the mixture was then heated to reflux for 2-3 hrs. After cooling to room temperature, H2O (100 ml) was added and the phases were separated. The aqueous phase was further extracted with CHCl3 (2×). The combined CHCl3 extractions were washed with sat'd NaCl (1×), dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by flash chromatography (1:1 hexanes:EtOAc, followed by 100% EtOAc) to give 7-benzyloxy-4-chloro-6-methoxy-quinoline (5.11 g, 48%). LC/MS Calcd for [M+H]+ 301.1, found 301.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476298B2
Source datasetuspto-grants-2013_07
ORD IDord-4c4275c5af654a33a77c536dd64af3ea
Source noteuspto-grants-2013_07