Phosgene → 5-Cyclopropyl-1,3,4-thiadiazol-2-yl isocyanate
Reaction equation
[C:1](Cl)(Cl)=[O:2].[CH:5]1([C:8]2[S:12][C:11]([NH2:13])=[N:10][N:9]=2)[CH2:7][CH2:6]1>C(OCC)(=O)C>[CH:5]1([C:8]2[S:12][C:11]([N:13]=[C:1]=[O:2])=[N:10][N:9]=2)[CH2:7][CH2:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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-cyclopropyl-2-amino-1,3,4-thiadiazole (6 grams) in ethyl acetate (100 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 filtered to recover the desired product 5-cyclopropyl-1,3,4-thiadiazol-2-yl isocyanate dimer.
Workup
- 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 filtered
- customto recover the desired product 5-cyclopropyl-1,3,4-thiadiazol-2-yl isocyanate dimer
Sources & evidence
- ORD record
- ord-6721fbf725584078b4240dd9c758ad2a
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04008068
Reaction notes
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