Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21831297 | HCID 21831297 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21831307 | HCID 21831307 | 96.1% |
Reaction Steps
To a mixture of 0.05 g of 6-pentafluoroethyl-2,2-bisfluoromethyl-4-(2-thioxo-1-pyrrolidinyl)-2H-1-benzopyran, 0.20 g of iodomethane, 0.05 g of cyanamide and 3 ml of tetrahydrofuran was added 0.06 g of sodium hydride (60%) under ice-cooling with stirring. The mixture was stirred under ice-cooling for 30 minutes and then stirred at room temperature for 17 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 49 mg of 4-(2-cyanoimino-1-pyrrolidinyl)-6-pentafluoroethyl-2,2-bisfluoromethyl-2H-1-benzopyran represented by the following formula having a melting point of 207-210°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977167 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-91e542d18a40479aacd38ba1ffacb150 |
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| Source note | uspto-grants-1999_11 |
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