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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018028Generated: October 30, 2026

Triethyl Phosphate → 5-Chloro-2,6-dimethoxy-4-methyl-8-nitroquinoline

https://huagongshe.com/reaction/1018028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantPotassium NitrateHCID 24434—
Reactant5-Chloro-2,6-dimethoxy-4-methylquinolineHCID 18405981—
SolventMethanolHCID 887—
Product5-Chloro-2,6-dimethoxy-4-methyl-8-nitroquinolineHCID 1096800568%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

A 20-liter reactor equipped with a mechanical stirrer, thermowatch, and condenser was charged with triethylphosphate (6.3 liters) and 2,6-dimethoxy-5-chloro-4-methylquinoline (5) (500 g, 2.11 moles). Phosphorous pentoxide (1.052 kg, 7.11 moles) was added in one portion and the resulting slurry stirred for 60 minutes. Reaction temperature was adjusted to 35° C. and solid potassium nitrate (0.423 kg, 4.21 moles) added in one portion. N-hexane is added and the reaction temperature was maintained at 35-40° C. for 2 hours. Methanol (4.2 liters) was added and the mixture heated to reflux and held for 1 hour. The yellow slurry was cooled to 0-5° C. and held for 2 hours. The product was collected by suction filtration, washed with water to neutral pH, then methanol, air dried and oven dried at 60-70° C. to yield the title compound 350 g (68%); mp 199-200° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479660B1
Source datasetuspto-grants-2002_11
ORD IDord-a48012aecff44ec6833a918f6091d8d0
Source noteuspto-grants-2002_11