Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (3-bromoprop-1-en-2-yl)benzene | HCID 234998 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19106821 | HCID 19106821 | 60.2% |
Reaction Steps
The compound, 2-aminothiophenol, (12.5 g) was added to a solution of sodium hydroxide (4.5 g) in ethanol (100 ml) keeping the temperature less than 30° C. Then 1-bromo-2phenyl-2-propene (21 g) was added and the mixture was stirred at 60° C. for 3 h. The precipitated solid was filtered and washed with ethanol. The solvent was removed and the residue was chromatographed on silica gel with hexanes/ethyl acetate (7:1) to yield the title compound (14.5 g). As an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05276039 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-560cbb259f4347eea88862b1489ab87f |
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| Source note | uspto-grants-1994_01 |
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