Morpholine → 4-(4-Trifluoromethylphenyl)morpholine

HRID 1313344Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1313344
C1COCCN1.FC(F)(F)c1ccc(Br)cc1>COCCOCCOC.C[Si](C)(C)[N-][Si](C)(C)C.O=S1C(c2ccccc2)=[C]2(c3ccccc3)->[Ni]3(<-[CH]4=CCC[CH]->3=CCC4)<-[C]1(c1ccccc1)=C2c1ccccc1.[Na+].c1ccc(P(C23CC4CC(CC(C4)C2)C3)C23CC4CC(CC(C4)C2)C3)c(N2CCCCC2)c1>FC(F)(F)c1ccc(N2CCOCC2)cc1

Komponenten

9

Edukt 2

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

Produkt 3

HCID 2519CaffeineHCID 109333104-(4-Trifluoromethylphenyl)morpholineAusbeute 18,02 %HCID 154202994-(3-(Trifluoromethyl)phenyl)morpholineAusbeute 15,176 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 2724254Sodium bis(trimethylsilyl)amideReagenzHCID 677145061-[2-[Bis(tricyclo[3.3.1.13,7]dec-1-yl)phosphino]phenyl]piperidineKatalysatorHCID 178527110HCID 178527110, VerbindungKatalysatorHCID 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-9bd432e153d14388bf9c38d13a1d9b98
Quelldatensatz
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
Originallink
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