HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 1-Methyl-5-(3-phenylthiopropyl)thio-1,2,3,4-tetrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methyl-5-(3-chloropropyl)thio-1,2,3,4-tetrazole | HCID 12803376 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Methyl-5-(3-phenylthiopropyl)thio-1,2,3,4-tetrazole | HCID 12818273 | 95.2% |
Reaction Steps
1-Methyl-5-(3-chloropropyl)thio-1,2,3,4-tetrazole (1.9 g) and thiophenol (1.1 g) are dissolved in acetone (50 ml). To the mixture are added potassium carbonate (1.5 g) and potassium iodide (0.1 g), and the mixture is refluxed for 3 hours. After acetone is distilled off, water is added to the residue, and the mixture is extracted with ether. The ether solution is washed with diluted aqueous sodium hydroxide and saturated aqueous sodium chloride and dried over sodium sulfate. After ether is distilled off, the residue is purified by silica gel column chromatography (Kieselgel 60), followed by eluting with benzene-chloroform (3:2) to give 1-methyl-5-(3-phenylthiopropyl)thio-1,2,3,4-tetrazole (2.5 g) as colorless liquid, nD18 =1.6008.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04372953 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-64e13d223ac54e87b14e07808855cda1 |
| Source note | uspto-grants-1983_02 |