HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 8-Amino-6-methoxy-4-methyl-5-(8-phenyloctoxy) quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Butyl ether | HCID 8909 | — |
| Reactant | 6-Methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline | HCID 54345436 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-Amino-6-methoxy-4-methyl-5-(8-phenyloctoxy) quinoline | HCID 54394829 | 61.1% |
Reaction Steps
A stirred mixture of 6-methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline (2.1 g, 0.005 mol), degreased 40 mesh Fe filings (5 g), H2O (20 ml), HOAc (4 ml) and n-Bu2O (4 ml) was heated at 80° C. to 1.5 h, cooled and filtered. The solid was thoroughly extracted with Et2O and the filtered extract was dried (Na2SO4), treated with carbon and concentrated to an oil. Trituration with pet ether gave 1.2 g (61%) of 8-amino-6-methoxy-4-methyl-5-(8-phenyloctoxy) quinoline as yellow-green solid, mp 33°-34° C. Crystallization from pet ether (Darco) gave the analytical sample as yellow green crystals, mp 39°-40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980360 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-e1e3b54f1b014628bc2b82556250e010 |
| Source note | uspto-grants-1990_12 |