HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propanethiol → 2-Isopropylthio-3-fluoropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propanethiol | HCID 6364 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Difluoropyridine | HCID 2783176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Isopropylthio-3-fluoropyridine | HCID 19966756 | 89.1% |
Reaction Steps
181.2 g of isopropylmercaptan are added dropwise at a temperature of 0° to +2° C. in the course of 25 minutes to a suspension of 324 g of anhydrous potassium carbonate and 335.6 g of 2,3-difluoropyridine in 4500 ml of dimethylformamide. After the reaction mixture has been stirred for 18 hours at room temperature, it is poured into a mixture of 8000 ml of ice-water and 4000 ml of ethyl acetate. The organic phase is subsequently separated off and washed with ice-water and then with ethyl acetate. The combined organic phases are dried with sodium sulfate and subsequently concentrated. Purification by column chromatography over silica gel with ethyl acetate/n-hexane (1:9) gives 362.9 g of 2-isopropylthio-3-fluoropyridine in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05352654 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-7f53ab5dbbbd4e15be5ff1b11eefc683 |
| Source note | uspto-grants-1994_10 |