Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Indole | HCID 798 | 32% |
Reaction Steps
A dry DMF solution of the compound (A-2) (0.01 mole) was added o-aminothiophenol (0.013 mole) and Ac2O (0.5ml) at room temperature. The mixture was stirred at 60° C. for 3 h. The reaction mixture was poured into stirred benzene and the precipitated solid was collected by filtration. The crude solid was washed with MeOH and recrystallized from benzene to afford target compound (A) (32% yield). 1H-NMR spectrum is shown in FIG. 3. Photoluminescence spectrum is shown in FIG. 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713194B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-ea6e5be525964d0ca63bb25dbda0176d |
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| Source note | uspto-grants-2004_03 |
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