HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → (E)-2-methyl-N-phenyl-3-(phenylthio)-2-propenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (E)-2-methyl-3-(phenylthio)-2-propenoic acid | HCID 13152781 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (E)-2-methyl-N-phenyl-3-(phenylthio)-2-propenamide | HCID 59498330 | 87% |
Reaction Steps
A suspension of 2.5 g (12.8 mmol) of (E)-2-methyl-3-(phenylthio)-2-propenoic acid and 3.5 g (25.7 mmol) of thionyl chloride in 25 ml of toluene was refluxed for 1 hour and then concentrated under vacuum. The residue was dissolved in 25 ml of ethyl acetate and cooled in ice bath. To the solution was added dropwise 2.9 g (32 mmol) of aniline and stirred at room temperature for 30 minutes. The reaction mixture was washed sequentially with 1N HCl solution, a saturated NaHCO3 solution, and a saturated NaCl solution. The organic layer was dried over anhydrous MgSO4 and concentrated to obtain 3.0 g of (E)-2-Methyl-N-phenyl-3-(phenylthio)-2-propenamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278473B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-e063550b00564276b337739f6f0504d9 |
| Source note | uspto-grants-2012_10 |