HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 67545329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | HCID 14397716 | HCID 14397716 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67545329 | HCID 67545329 | — |
Reaction Steps
To a solution of 201 mg of phenyl 3,N-diphenylpropynimidothioate in 5 ml of THF was added 0.08 ml of thiophenol and tert-butoxy potassium (a catalytic amount). The mixture was stirred at room temperature for 2 hours and then refluxed for 2 hours. The reaction mixture was concentrated under vacuum. The residue was purified by medium pressure preparative HPLC to obtain 269 mg of phenyl 3,N-diphenyl-3-(phenylthio)-2-propenimidothioate (hereinafter referred to as the present compound 42) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278473B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-e37a4fd578db4bec8dfa26c3a564b6ae |
| Source note | uspto-grants-2012_10 |