Morpholine → 4-(4-Trifluoromethylphenyl)morpholine

HRID 1325796Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1325796
C1COCCN1.FC(F)(F)c1ccc(Br)cc1>CC(C)(C)[O-].CC(C)n1cc[n+](C(C)C)c1.COCCOCCOC.CS(C)=O.[Cl-].[Cu][O][Cu].[Na+]>FC(F)(F)c1ccc(N2CCOCC2)cc1

Komponenten

10

Edukt 2

HCID 8083MorpholineHCID 67872Benzene, 1-bromo-4-(trifluoromethyl)-

Produkt 3

HCID 2519CaffeineHCID 109333104-(4-Trifluoromethylphenyl)morpholineAusbeute 2,22 %HCID 154202994-(3-(Trifluoromethyl)phenyl)morpholineAusbeute 0 %

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 23676156Sodium t-butoxideReagenzHCID 112292421,3-Diisopropylimidazolium chlorideKatalysatorHCID 178505380HCID 178505380, VerbindungKatalysatorHCID 679Dimethyl SulfoxideLösungsmittel5×HCID 8150DiglymeLösungsmittel5×

Reaktionsbedingungen

Temperatur
60 °C

Aufarbeitung

  1. customThe foil sealing tape was removed from the plate.
  2. addition3 μL of a 0.0667 M solution of caffeine in DMSO was added to each reaction well using an SPT Labtech Mosquito® liquid handling robot
  3. filtrationThe plates were then centrifuged for 15 to 20 seconds. · liquid-Phase beibehalten
  4. aliquotFollowing centrifugation, 500 nL of the resultant mixture from each well was carefully dispensed into four 384-well analytical plates (Analytical Sales # 38435) using an SPT Labtech Mosquito® liquid handling robot. Each well of these analytical plates contained 30 μL of DMSO with 0.1% acetic acid, pre-dosed by OpenTrons, to facilitate analysis.

Quellen und Nachweise

ORD-Eintrag
ord-d05a0a80b8bc44618238d3f6d54215c8
Quelldatensatz
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
Originallink
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