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Morpholine → 4-(4-Trifluoromethylphenyl)morpholine

HRID 1322487
Notes
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Reaction equation

HRID 1322487 reaction equation
C1COCCN1.FC(F)(F)c1ccc(I)cc1>CS(C)=O.O=C([O-])[O-].[Cl-].[Cl][Cu].[Cs+].c1c[n+](C2CCCCC2)cn1C1CCCCC1>FC(F)(F)c1ccc(N2CCOCC2)cc1
ParticipantsConditionsWorkupSources & evidenceReaction notes

Participants

9

Reactant 2

HCID 8083MorpholineHCID 67993Benzene, 1-iodo-4-(trifluoromethyl)-

Product 3

HCID 2519CaffeineHCID 109333104-(4-Trifluoromethylphenyl)morpholineYield 0%HCID 154202994-(3-(Trifluoromethyl)phenyl)morpholineYield 0%

Reagents, catalysts & solvents 4

HCID 14794698CID 14794698ReagentHCID 62652Cuprous chlorideCatalystHCID 109565421,3-Dicyclohexyl-imidazolium chlorideCatalystHCID 679Dimethyl SulfoxideSolvent5×

Conditions

Temperature
80 °C

Workup

  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. · Keep liquid
  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.

Sources & evidence

ORD record
ord-5362b915381a4963b115d8944351773b
Source dataset
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
DOI
10.1021/jacs.6c05959
Original link
View source

Reaction notes

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On this pageParticipantsConditionsWorkupSources & evidenceReaction notes