Methanethiol → HCID 178484946, Verbindung
Reaktionsgleichung
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[IH:10].[CH3:11][NH:12][C:13](=[N:16][CH3:17])SC.CS>C(O)C>[IH:10].[CH3:11][NH:12][C:13]([NH:16][CH3:17])=[N:9][CH2:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-phenylethylamine (2.4 g.), N,N',S-trimethylisothiourea hydriodide (4.92 g.) and ethanol (70 ml.), were boiled together under reflux for eight hours; methyl mercaptan was evolved. The resulting solution was evaporated to dryness and the residue recrystallised from methanol/ether mixture to yield N,N'-dimethyl-N"-2-phenylethylguanidine hydriodide, melting point 156°-160°C.
Aufarbeitung
- temperatureunder reflux for eight hours
- customThe resulting solution was evaporated to dryness
- customthe residue recrystallised from methanol/ether mixture
Quellen und Nachweise
- ORD-Eintrag
- ord-f4ee57d54bcb4c648d3450532234631c
- Quelldatensatz
- uspto-grants-1976_07
- Patentnummer
- US03968243
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