Methyl iodide → HCID 73847915, compound
Reaction equation
[F:1][C:2]([F:27])([C:7]1[CH:8]=[CH:9][C:10]2[O:15][C:14]([CH2:18][F:19])([CH2:16][F:17])[CH:13]=[C:12]([N:20]3[CH2:24][CH2:23][CH2:22][C:21]3=S)[C:11]=2[CH:26]=1)[C:3]([F:6])([F:5])[F:4].IC.[N+:30]([CH3:33])([O-:32])=[O:31].[H-].[Na+]>O1CCCC1>[F:1][C:2]([F:27])([C:7]1[CH:8]=[CH:9][C:10]2[O:15][C:14]([CH2:18][F:19])([CH2:16][F:17])[CH:13]=[C:12]([N:20]3[CH2:24][CH2:23][CH2:22][C:21]3=[CH:33][N+:30]([O-:32])=[O:31])[C:11]=2[CH:26]=1)[C:3]([F:6])([F:5])[F:4]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a mixture of 0.16 g of 6-pentafluoroethyl-2,2-bisfluoromethyl-4-(2-thioxo-1-pyrrolidinyl)-2H-1-benzopyran, 0.78 g of iodomethane, 0.41 g of nitromethane and 6 ml of tetrahydrofuran was added 0.10 g of sodium hydride (60%) at room temperature with stirring. The mixture was refluxed with heating for 2 hours. After addition of ice water, the mixture was extracted with methylene chloride. The organic layer was washed with water and dried. The solvent was distilled off and the resultant residue was purified using silica gel column chromatography (developing solution, MeOH:CH2Cl2 =1:99) to obtain 0.02 g of 6-pentafluoroethyl-2,2-bisfluoromethyl-4-(2-nitromethylene-1-pyrrolidinyl)-2H-1-benzopyran represented by the following formula having a melting point of 195°-197° C.
Workup
- temperatureThe mixture was refluxed
- temperaturewith heating for 2 hours
- extractionthe mixture was extracted with methylene chloride
- washThe organic layer was washed with water
- customdried
- distillationThe solvent was distilled off
- customthe resultant residue was purified
Sources & evidence
- ORD record
- ord-2297555a03a44571b11652e525d16363
- Source dataset
- uspto-grants-1999_02
- Patent number
- US05874446
Reaction notes
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