Reaktionsgleichung
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1F)[C:6]#[N:7].[NH:14]([CH2:18][CH2:19][OH:20])[CH2:15][CH2:16][OH:17]>CN(C)C(=O)C>[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[N:14]([CH2:18][CH2:19][OH:20])[CH2:15][CH2:16][OH:17])[C:6]#[N:7]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 3-trifluoromethyl 4-fluoro-benzonitrile (9.45 g, 50 mmol) and diethanolamine (15.8 g, 0.15 mol) in N,N-dimethylacetamide (200 ml) was stirred for 7 days at 50° C. The solvent was evaporated, the residue partitioned between CH2Cl2 (400 ml) and H2O (400 ml), the organic layer dried (MgSO4) and evaporated to dryness. The residue was chromatographed using CH2Cl2-EtOH as eluent.
Aufarbeitung
- customThe solvent was evaporated
- customthe residue partitioned between CH2Cl2 (400 ml) and H2O (400 ml)
- dry with materialthe organic layer dried (MgSO4)
- customevaporated to dryness
- customThe residue was chromatographed
Quellen und Nachweise
- ORD-Eintrag
- ord-02ab42cfd43b416bbf1faed23df2983f
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06852755B1
Verknüpfte Notizen
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