HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenethiol, pentafluoro- → 2-{[(Pentafluorophenyl)sulfanyl]methyl}pyridine--hydrogen chloride (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenethiol, pentafluoro- | HCID 13042 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Picolyl chloride hydrochloride | HCID 23392 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-{[(Pentafluorophenyl)sulfanyl]methyl}pyridine--hydrogen chloride (1/1) | HCID 12760224 | 61.1% |
Reaction Steps
Pentafluorothiophenol (5 g) was added to a solution of sodium hydroxide (2.0 g) in ethanol (50 ml) and the resulting solution was treated with a solution of 2-picolyl chloride, hydrochloride (4.1 g) in ethanol (25 ml). The mixture was stirred at ambient temperature for 4 hours, filtered through Kieselghur and the solvent removed by evaporation. The residue was converted into the hydrochloride with ethereal HCl solution and this was recrystallised from acetone-ether to give 2-(((pentafluorophenyl)thio)methyl)pyridine, hydrochloride (5.0 g) mp 157°-8° C. (Found: C,44.0; H,2.4; N,4.0; C12H6F5NS.HCl requires C,44.0; H,2.15; N,4.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04327102 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-e03f2db398654eb49c135beb30923a74 |
| Source note | uspto-grants-1982_04 |