Phosgene → 2-Isocyanato-5-(trifluoromethyl)-1,3,4-thiadiazole
Reaction equation
[C:1](Cl)(Cl)=[O:2].[F:5][C:6]([F:14])([F:13])[C:7]1[S:8][C:9]([NH2:12])=[N:10][N:11]=1>C(OCC)(=O)C>[F:5][C:6]([F:14])([F:13])[C:7]1[S:8][C:9]([N:12]=[C:1]=[O:2])=[N:10][N:11]=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 2-trifluoromethyl-5-amino-1,3,4-thiadiazole (45 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 filtered to recover 48 grams of a white solid. This solid was recrystallized from dimethyl formamide to yield the desired product 2-trifluoromethyl-1,3,4-thiadiazol-5-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 48 grams of a white solid
- customThis solid was recrystallized from dimethyl formamide
Sources & evidence
- ORD record
- ord-f63ad0f9e8b54a57a755720fca48d86c
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03951640
Reaction notes
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