Bleirhodanid → {[(2,2,2-Trichloroethoxy)carbonyl]amino}acetyl isothiocyanate
Reaktionsgleichung
[Cl:1][C:2]([Cl:13])([Cl:12])[CH2:3][O:4][C:5]([NH:7][CH2:8][C:9](Cl)=[O:10])=[O:6].[Pb](SC#N)[S:15][C:16]#[N:17]>C1(C)C=CC=CC=1>[Cl:1][C:2]([Cl:13])([Cl:12])[CH2:3][O:4][C:5]([NH:7][CH2:8][C:9]([N:17]=[C:16]=[S:15])=[O:10])=[O:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 20 parts of the preceeding acetyl chloride and 30 parts of lead thiocyanate in 150 parts by volume of toluene is refluxed for about 4 hours, then cooled to ambient temperature and filtered. The solvent is removed from the filtrate and the remaining oil distilled using fractionating column under vacuum to give {[(2,2,2-trichloroethoxy)carbonyl]amino}acetyl isothiocyanate. This compound is represented by the following formula
Aufarbeitung
- filtrationfiltered
- customThe solvent is removed from the filtrate
- distillationthe remaining oil distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-021e2d4423f54e37941da6f8ca876973
- Quelldatensatz
- uspto-grants-1980_06
- Patentnummer
- US04208327
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