HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Cyanomethyl 2-(cyanomethylthio)nicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 178524460 | HCID 178524460 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cyanomethyl 2-(cyanomethylthio)nicotinate | HCID 2532264 | — |
Reaction Steps
12 Grams (0.16 mole) of chloroacetonitrile was added to a stirred suspension of 6.2 g (0.04 mole) of 2-mercaptonicotinic acid, 8.0 g (0.08 mole) of potassium bicarbonate, and 20 g (0.12 mole) of potassium iodide in 100 ml of dimethylformamide at 10° under nitrogen. The reaction was stirred at 10° for 7 hr., then at 25° for 15 hr. The reaction mixture was then poured into water, saturated with sodium chloride and filtered. The resulting solid was dissolved in methylene chloride, dried with magnesium sulfate and evaporated to give 7.5 g of cyanomethyl 2-(cyanomethylthio)nicotinate. m.p. 140°-143° C. NMR (DMSO) δ3.3(s,2); 4.3(s,2); 6.4(dd,1); 7.4(dd,1); 7.8(dd,1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220776 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-db111377924643b9a7c91b19da1e9bd3 |
| Source note | uspto-grants-1980_09 |