Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Propyne, 3-(chloromethoxy)- | HCID 12241341 | — |
| Reactant | HCID 178477412 | HCID 178477412 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23368330 | HCID 23368330 | — |
Reaction Steps
1.86 Grams of 3-hydroxy-4-cyano-5-ethylthioisothiazole was dissolved in 30 ml of DMF, and 0.7 g of potassium carbonate was added thereto. Thereafter, 1.3 g of 2-propynyloxymethyl chloride was added at room temperature with stirring, and the reaction solution was stirred at 50° C. for 2 hours. The reaction solution was ice-cooled to 5° to 10° C., a solution of 5.0 g of iodine and 3.2 g of potassium iodide in 5 ml of water and 20 ml of DMF was added thereto, and then 6.6 g of 10% KOH was added dropwise. After addition, the reaction solution was stirred at room temperature for 1 hour. Water was added to the reaction solution, which was then extracted with ethyl acetate. The extract was washed with water, dried and concentrated under reduced pressure to obtain crude crystals. Recrystallization of the crude crystals from ether/hexane gave 2.6 g of crystals having a melting point of 57° to 58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05578622 |
|---|
| Source dataset | uspto-grants-1996_11 |
|---|
| ORD ID | ord-206ec59a533a485081bcfa7752100355 |
|---|
| Source note | uspto-grants-1996_11 |
|---|