HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Fluoroaniline → 1-Acetyl-2-methyl-4-[(2-fluorophenyl)imino]-1,2,3,4-tetrahydroquinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Fluoroaniline | HCID 9584 | — |
| Edukt | 4(1H)-Quinolinone, 1-acetyl-2,3-dihydro-2-methyl- | HCID 589563 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-Acetyl-2-methyl-4-[(2-fluorophenyl)imino]-1,2,3,4-tetrahydroquinoline | HCID 66625241 | 82,3% |
Reaktionsschritte
[Step 1] 50 mg of 1-acetyl-4-oxo-2-methyl-1,2,3,4-tetrahydroquinoline and 83 mg of 2-fluoroaniline were dissolved in 2 mL of toluene, and 125 μL of titanium tetrachloride (1.0 M dichloromethane solution) was added to the solution under ice cooling. The resulting mixture was stirred for one hour under ice cooling, and then was stirred for 3 hours at 80° C. After completion of the reaction, the reaction liquid was filtered through Celite and was concentrated under reduced pressure. The resulting residue was purified by using silica gel chromatography (diethyl ether:hexane=2:1), and thus 60 mg (81%) of 1-acetyl-2-methyl-4-[(2-fluorophenyl)imino]-1,2,3,4-tetrahy droquinoline was obtained as a yellow oily substance.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09045423B2 |
| Quelldatensatz | uspto-grants-2015_06 |
| ORD ID | ord-53075a29a7834672bc889afd392c3c78 |
| Quellennotiz | uspto-grants-2015_06 |