Reaktionsgleichung
[NH:1]1[CH2:5][CH2:4][CH2:3][C:2]1=[O:6].[H-].[Na+].[I:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14]Br)=[CH:12][CH:11]=1>CN(C=O)C>[I:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][N:1]2[CH2:5][CH2:4][CH2:3][C:2]2=[O:6])=[CH:12][CH:11]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 140 μl (1.68 mmol) 2-pyrrolidone in 5 mL DMF are added 110 mg (2.53 mmol) sodium hydride. Then 500 mg (1.68 mmol) 4-iodobenzyl bromide are added by several portions and the resulting mixture is stirred at r.t. over night. The solvent is removed in vacuo and the residue is resolved in DCM and water. The layers are separated and the organic layer is dried with Na2SO4, filtrated and the solvent is removed in vacuo. The crude product is purified by HPLC.
Aufarbeitung
- customThe solvent is removed in vacuo
- customThe layers are separated
- dry with materialthe organic layer is dried with Na2SO4
- filtrationfiltrated
- customthe solvent is removed in vacuo
- customThe crude product is purified by HPLC
Quellen und Nachweise
- ORD-Eintrag
- ord-392c23370f18485ea0366c42b5d658a8
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08835472B2
Verknüpfte Notizen
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