HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-[N-(6-chloro-2-quinolinyl)-N-methylamino]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,6-Dichloroquinoline | HCID 607502 | — |
| Reactant | p-(N-methylamino)phenol sulfate | HCID 10198132 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[N-(6-chloro-2-quinolinyl)-N-methylamino]phenol | HCID 20461960 | — |
Reaction Steps
A mixture of 2,6-dichloroquinoline (1.1 g; prepared according to the method of O Fischer, Chem. Ber., 35, 3683 (1902), 4-(N-methylamino)phenol sulfate (1.5 g), ethanol (5 ml) and water (20 ml) was heated under reflux for a period of 24 hours. Water (50 ml) was added to the mixture and the aqueous mixture was extracted with chloroform (2×100 ml). The chloroform extracts were dried (anhydrous MgSO4) and the solvent was evaporated to give 4-[N-(6-chloro-2-quinolinyl)-N-methylamino]phenol (1.1 g) as a dark oil. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 8.0-6.6 and 7.2 (10H, m and d of d, quinoline, hydroxy and phenyl protons); 3.6 (3H, s, N--CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04444584 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-37489c974622447eb1ccd989ce18ad71 |
| Source note | uspto-grants-1984_04 |