Morpholine → 4-(4-Trifluoromethylphenyl)morpholine

HRID 1301654

反応式

HRID 1301654 の反応式
C1COCCN1.FC(F)(F)c1ccc(Br)cc1>CC1=CC(C)=O->[Pd]2(O1)OC(C)=CC(C)=O->2.C[Si](C)(C)[O-].[Li+].COCCOCCOC.COCCOCCOC.COCCOCCOC.COCCOCCOC.COCCOCCOC>Cn1c(=O)c2c(ncn2C)n(C)c1=O.FC(F)(F)c1ccc(N2CCOCC2)cc1.FC(F)(F)c1cccc(N2CCOCC2)c1

参加物

8

反応物 2

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

生成物 3

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

試薬・触媒・溶媒 3

HCID 74821Lithium trimethylsilanolate試薬HCID 178427257HCID 178427257、化合物触媒HCID 8150Diglyme溶媒5 回

反応条件

温度
60 °C

後処理

  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 相を保持
  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.

出典と根拠

ORDレコード
ord-806fdad7c61f4413bccc8f6630101363
出典データセット
High-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
元リンク
出典を表示

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