Phenacyl bromide → HCID 178444626, Verbindung

HRID 1812484

Reaktionsgleichung

Reaktionsgleichung von HRID 1812484
C#CCCCCC=O.c1ccc(C(=O)CBr)cc1>C[Si](C)(C)OC(c1ccccc1)(c1ccccc1)[C@@H]1CCCN1.[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].Cl[Ru]Cl.c1ccc(nc1)-c2ccccn2.c3ccc(nc3)-c4ccccn4.c5ccc(nc5)-c6ccccn6.CN(C)C=O.Cc1cccc(C)n1>C#CCCC[C@@H](C=O)CC(=O)c1ccccc1.C#CCCC[C@H](C=O)CC(=O)c1ccccc1

Komponenten

8

Edukt 3

HCID 6259Phenacyl bromideHCID 79372,6-LutidineHCID 11355455Hept-6-ynal

Produkt 2

HCID 178444626HCID 178444626, VerbindungHCID 178444627HCID 178444627, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 11198150(S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl EtherKatalysatorHCID 16211607Tris(2,2-bipyridyl)ruthenium(II) chloride hexahydrateKatalysatorHCID 6228DimethylformamideLösungsmittel5×

Reaktionsbedingungen

Temperatur
22 °C

Aufarbeitung

  1. aliquot4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN
  2. addition4 uL mixture of each reacted solution was collected and diluted with 36 uL ACN
  3. additionchiral resolving regent (150 mM in DCM, 40 uL)
  4. additionCuI with DIPEA (400 mM in ACN) 40 uL
  5. additioninternal standard 1-phenylprop-2-yn-1-ol (4) (25 mM in ACN) 40 uL
  6. stirringKeine Vorschrift aufgezeichnet
  7. aliquotAfter the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate
  8. additionAfter the reaction, 10 uL of supernatant for each reaction was transferred to another 96-well plate and diluted with 190 uL ACN before the IM-MS analysis

Quellen und Nachweise

ORD-Eintrag
ord-ab72a1b17c2a4b34a7f3ec52b3f02495
Quelldatensatz
Dataset from `Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery`

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