Methyl iodide → HCID 178503994, compound
Reaction equation
[CH3:1][I:2].[F:3][C:4]([F:16])([F:15])[C:5]1[CH:6]=[C:7]([NH:11][C:12]([NH2:14])=[S:13])[CH:8]=[CH:9][CH:10]=1>O1CCOCC1>[IH:2].[F:16][C:4]([F:3])([F:15])[C:5]1[CH:6]=[C:7]([NH:11][C:12](=[NH:14])[S:13][CH3:1])[CH:8]=[CH:9][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The starting material for this synthesis is produced as follows: 8 g of methyl iodide in 20 ml of dioxane is added to a solution of 11 g of N-(m-trifluoromethylphenyl)thiourea in 30 ml of dioxane. The reaction mixture is heated for 3 hours on a water bath. The dioxide is evaporated off under reduced pressure, and the residue is recrystallised from a mixture of isopropanol and ethyl acetate to yield N-(m-trifluoromethylphenyl)-S-methylisothiourea-hydroiodide, which melts at 220°.
Workup
- customThe starting material for this synthesis is produced
- temperatureThe reaction mixture is heated for 3 hours on a water bath
- customThe dioxide is evaporated off under reduced pressure
- customthe residue is recrystallised from a mixture of isopropanol and ethyl acetate
Sources & evidence
- ORD record
- ord-7daf8aef9f6747369b4c3a2b44bbf76f
- Source dataset
- uspto-grants-1986_12
- Patent number
- US04626537
Reaction notes
Loading…