Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030189Generated: November 4, 2026

Propylene Oxide → 6-Methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline

https://huagongshe.com/reaction/1030189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene OxideHCID 6378—
ReactantHexamethylphosphoramideHCID 12679—
Reactant(8-Bromooctyl)benzeneHCID 563758—
Reactant4-Methyl-5-hydroxy-6-methoxy-8-nitroquinolineHCID 135778511—
SolventTriethylamineHCID 8471—
Product6-Methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinolineHCID 5434543660.6%

Reaction Steps

To a stirred mixture of 5-hydroxy-6-methoxy-4-methyl-8-nitroquinoline (4.98 g, 0.02 mol), 1-bromo-8-phenyloctane (4.7 g, 0.017 mol) and HMPA (13 ml), at 120° C., was added, dropwise, during 1 h, a mixture of propylene oxide (6 ml) and Et3N (1 ml). The reaction was continued for 3.5 h, allowed to cool and extracted successively with pet ether, Et2O and Me2CO leaving 1 g of insoluble starting material, 5-hydroxy-6-methoxy-4-methyl-8-nitroquinoline. The combined pet ether and Et2O extracts were washed (H2O, dil NaOH, H2O), dried (Na2SO4) and concentrated. The residue was dissolved in CHCl3, placed on silica gel column and eluted with CHCl3. Concentration of the eluates left an oil which was triturated with pet ether to give 4.35 g (60%) of 6-methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline as yellow solid, mp 39.5°-41° C. Crystallization from hexane (Darco) provided the analytical sample as yellow crystals, mp 41°-42° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104885
Source datasetuspto-grants-1992_04
ORD IDord-ff3ea77e1768405094f4c09a8a8ed16d
Source noteuspto-grants-1992_04