HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 8-Amino-6-methoxy-4-methyl-5-(4-phenylbutoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Butyl ether | HCID 8909 | — |
| Reactant | 6-Methoxy-4-methyl-8-nitro-5-[4-phenylbutoxy]quinoline | HCID 563517 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-Amino-6-methoxy-4-methyl-5-(4-phenylbutoxy)quinoline | HCID 609145 | 66% |
Reaction Steps
A stirred mixture of 6-methoxy-4-methyl-8nitro-5-(4-phenylbutoxy) quinoline (3.7 g, 0.01 mol), degreased 40mesh Fe filings (10 g), H2O (40 ml), HOAc (8 ml) and Bu2O (8 ml) was heated at 80°-100° C. for 2.5 h, allowed to cool and filtered. The solid was thoroughly extracted with Et2O and the extract was dried (Na2SO4), treated with carbon and concentrated to an oil. Extraction of the latter with pet ether and cooling the extract gave 2.2 g (66%) of 8-amino-6methoxy-4-methyl-5-(4-phenylbutoxy)quinoline as yellow-green crystals, mp 59°-59.5° C. Recrystallization from pet ether afforded the analytical sample as yellow crystals, mp 60°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980360 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-e1e7ddb3fc28425cb074cde3b859a77e |
| Source note | uspto-grants-1990_12 |