Phosgene → 2-t-Butyl-1,3,4-thiadiazol-5-yl Isocyanate
Reaktionsgleichung
[C:1](Cl)(Cl)=[O:2].[C:5]([C:9]1[S:13][C:12]([NH2:14])=[N:11][N:10]=1)([CH3:8])([CH3:7])[CH3:6]>C(OCC)(=O)C>[C:5]([C:9]1[S:13][C:12]([N:14]=[C:1]=[O:2])=[N:11][N:10]=1)([CH3:8])([CH3:7])[CH3:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A saturated solution of phosgene in ethyl acetate (100 ml) was charged into a glass reaction vessel equipped with a mechanical stirrer. A slurry of 5-t-butyl-2-amino-1,3,4-thiadiazole (10 grams) in ethyl acetate (300 ml) was added to the reaction vessel, and the resulting mixture was stirred for a period of about 16 hours, resulting in the formation of a precipitate. The reaction mixture was then purged with nitrogen gas to remove unreacted phosgene. The purged mixture was then filtered to recover the desired product 5-t-butyl-1,3,4-thiadiazol-2-yl isocyanate dimer as a solid having a melting point of 261° to 263° C.
Aufarbeitung
- customequipped with a mechanical stirrer
- customresulting in the formation of a precipitate
- customThe reaction mixture was then purged with nitrogen gas
- customto remove unreacted phosgene
- filtrationThe purged mixture was then filtered
- customto recover the desired product 5-t-butyl-1,3,4-thiadiazol-2-yl isocyanate dimer as a solid
Quellen und Nachweise
- ORD-Eintrag
- ord-904f18dc5242444e9b3e8f96b92eca1c
- Quelldatensatz
- uspto-grants-1977_07
- Patentnummer
- US04033753
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