Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111394Generated: October 30, 2026

Propylene Oxide → 6-Methoxy-4-methyl-8-nitro-5-(9-phenylnonoxy) quinoline

https://huagongshe.com/reaction/1111394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene OxideHCID 6378—
ReactantHexamethylphosphoramideHCID 12679—
ReactantBenzene, (9-bromononyl)-HCID 11119579—
Reactant4-Methyl-5-hydroxy-6-methoxy-8-nitroquinolineHCID 135778511—
SolventTriethylamineHCID 8471—
Product6-Methoxy-4-methyl-8-nitro-5-(9-phenylnonoxy) quinolineHCID 5403028332.1%

Reaction Steps

To a stirred mixture of 5-hydroxy-6methoxy-4methyl-8nitroquinoline (4.7 g, 0.02 mol), 1 bromo-9-phenylnonane (4.2 g, 0.015 mol) and HMPA (10 ml), at 125- 130° C., was added dropwise, during 0.5 h, a mixture of propylene oxide (6 ml) and Et3N (1 ml). The reaction was continued for 6 h, allowed to cool and extracted successively with pet ether, Et2O and Me2CO leaving 1.9 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 residual oil was dissolved in CHCl3, placed on a silica gel column (100 g) and eluted with CHCl3. The eluates were concentrated, triturated with pet ether and crystallized from Et2O (Darco) to give 2.1 g of 6-methoxy-4-methyl-8-nitro-5 -(9-phenylnonoxy) quinoline as yellow crystals, mp 56°-56.5° C. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980360
Source datasetuspto-grants-1990_12
ORD IDord-3d25e2363d1d41229740610c53c65e4c
Source noteuspto-grants-1990_12