4-(Trifluoromethyl)phenyl isothiocyanate → HCID 18351910, compound
Reaction equation
[N:1]#[C:2][NH2:3].[Na].[F:5][C:6]([F:17])([F:16])[C:7]1[CH:12]=[CH:11][C:10]([N:13]=[C:14]=[S:15])=[CH:9][CH:8]=1>C(O)C>[C:2]([NH:3][C:14]([NH:13][C:10]1[CH:9]=[CH:8][C:7]([C:6]([F:5])([F:16])[F:17])=[CH:12][CH:11]=1)=[S:15])#[N:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The suspension of monosodium cyanamide (0.63 g, 9.8 mmol) in absolute ethanol (50 mL) was slowly treated with 4-trifluoromethylphenylisothiocyanate (2.0 g, 9.8 mmol). The reaction was allowed to stir at room temperature for 1 hour and then heated at 75° C. for 4 hours. The reaction was cooled to room temperature and the colorless solid was filtered and washed with ethanol to give the title compound (2.0 g) as a colorless solid.
Workup
- temperatureheated at 75° C. for 4 hours
- temperatureThe reaction was cooled to room temperature
- filtrationthe colorless solid was filtered
- washwashed with ethanol
Sources & evidence
- ORD record
- ord-322ed0b20bbc43b1afd3b0cb1e4a473c
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05140031
Reaction notes
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