3,5-Dimethylbenzoic acid → N-methoxy-N,3,5-trimethylbenzamide
Reaktionsgleichung
CNOC.Cc1cc(C)cc(C(=O)O)c1.CN(C)C(=[N+](C)C)F.F[P-](F)(F)(F)(F)F.CN(C)C1=CC=NC=C1.CCN(C(C)C)C(C)C.CN(C)C=O>>CON(C)C(=O)c1cc(C)cc(C)c1Komponenten
7
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 4
Reaktionsbedingungen
- Temperatur
- 25 °C
Aufarbeitung
- addition150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
- addition150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
- aliquot10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
- addition380 uL MeCN solvent were added to the transfer plate
- aliquot20 uL taken from transfer plate to filter plate 1 for LCMS analysis
- addition180 uL MeCN added to filter plate 1 for LCMS analysis
- aliquot10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
- addition190 uL MeCN added to filter plate 2 for TOF-DESI analysis
- customthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM
Quellen und Nachweise
- ORD-Eintrag
- ord-8fde81e2e1044f07b8f53eeef6257d64
- Quelldatensatz
- AIChemEco amide coupling conditions 47k dataset
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