Reaktionen der Dialkylcyanamide (I) mit SOCl2 und analog des Cyanamids (Ia) mit d Iminothionylchloriden (III) bei 0‐20°C liefern praktisch quantitativ die N‐Chlorsulfin irninocarbaminsäurechloride (II) bzw. die N‐Chloriminosulfinyl‐iminocarbaminsäure‐ Chloride (IV).
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