Sodium Chloride → HCID 178510797, Verbindung
Reaktionsgleichung
[ClH:1].[C:2]1([CH2:8][C:9]([NH2:11])=[NH:10])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[O-].[Na+].[Cl-].[Na+]>O>[Cl:1][NH:10][C:9](=[NH:11])[CH2:8][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
The crude 2-phenyl-acetamidine hydrochloride (1.32 g, 7.74 mmol) was dissolved in water (10 mL) and cooled to 0° C. A ˜1.7 M solution of sodium hypochlorite in water (3.68 mL, 6.26 mmol) was added dropwise. The reaction mixture was stirred 1 h, then solid sodium chloride was added to saturate the aqueous phase, which was extracted with ethyl acetate (2×25 mL). The combined organic phases were filtered through sodium sulfate and evaporated in vacuo. The residue was purified by flash column chromatography (Merck silica gel 60, 40-63 μm; 33% ethyl acetate/hexanes) to afford N-chloro-2-phenyl-acetamidine (155 mg, 9% over two steps) as an off-white semi-solid: H1-NMR (400 MHz, CDCl3) δ=3.67 (2H, s), 5.13 (2H, br), 7.31 (5H, m).
Aufarbeitung
- concentrationto saturate the aqueous phase, which
- extractionwas extracted with ethyl acetate (2×25 mL)
- filtrationThe combined organic phases were filtered through sodium sulfate
- customevaporated in vacuo
- customThe residue was purified by flash column chromatography (Merck silica gel 60, 40-63 μm; 33% ethyl acetate/hexanes)
Quellen und Nachweise
- ORD-Eintrag
- ord-7c6931135a4b4dd79f33657a679521a3
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07902248B2
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