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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | (8-Bromooctyl)benzene | HCID 563758 | — |
| Reactant | 4-Methyl-5-hydroxy-6-methoxy-8-nitroquinoline | HCID 135778511 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline | HCID 54345436 | 60.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104885 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-ff3ea77e1768405094f4c09a8a8ed16d |
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| Source note | uspto-grants-1992_04 |
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