Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 22597171 | HCID 22597171 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22597170 | HCID 22597170 | — |
Reaction Steps
A 500 ml three neck round bottom flask was equipped with a mechanical stirrer, heating mantle and condenser. To the flask was added 52.5 g (0.11 mole) of 3-bromo-2-(1-isobutyl-3-methylbutoxy)-7H-benzo[de]anthracene-7-one (4), 9.2 g (0.087 mole) sodium carbonate, 16.0 g (0.13 mole) 2-aminothiophenol and 170 g DMF. The mixture was agitated well and heated at 120-130° C. for three hours. The reaction was cooled to 25° C. and 300 g water was added. The reaction mixture was extracted twice with 250 g chloroform. The organic layers were combined and washed twice with 250 g water. The solvent was removed on a rotary evaporator. The yield of crude product was 55 g of a dark brown oil which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531613B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-ba8da0f1fdd1480898a7cbe595237636 |
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| Source note | uspto-grants-2003_03 |
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