HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5,6,7,8-Tetrahydro-7-(methylamino)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanamine, hydrochloride (1:1) | HCID 11637 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5,6-Dihydroquinoline | HCID 12318317 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Toluene ethylacetate | HCID 21584019 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5,6,7,8-Tetrahydro-7-(methylamino)quinoline | HCID 14835921 | 83.2% |
Reaction Steps
A solution of methylammonium chloride (1.35 g, 20 mmol) in methanol (2 ml) was added to 5,6-dihydroquinoline (1.31 g, 10 mmol) in methanol (2 ml) and the solution was heated under reflux for 21h, poured onto a mixture of water (25 ml) and brine (25 ml), and basified with 10N-NaOH (25 ml). The mixture was extracted with chloroform (3×25 ml), and the extracts were dried (Na2SO4) and concentrated in vacuo to give an orange oil. Chromatography [alumina; ethyl acetate-toluene (1:4)→ethyl acetate] gave the product (1.35 g) as an oil which was identical to the compound isolated in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075303 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-8fed0ceb97524b93b7d35b54634c528a |
| Source note | uspto-grants-1991_12 |