HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111392Generated: October 27, 2026
Propylene Oxide → 6-Methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline
https://huagongshe.com/reaction/1111392
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-4methyl-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 a 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 | US04980360 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-584e83ea3cec4498a9df48b9932e3392 |
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| Source note | uspto-grants-1990_12 |
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