Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54468138 | HCID 54468138 | 55.4% |
Reaction Steps
To 44.8 g of 6-bromo-2-naphthol were added 120 ml of toluene and 8.8 g of sodium hydroxide, followed by stirring at 65° C. for 30 minutes. Then, thereto was added dropwise 11.4 g of acrylonitrile at 80° C., followed by stirring at the same temperature for 3.5 hours. After left for cooling, the toluene layer was decanted, and to the residue was added 240 ml of water. A small amount of insoluble matter was filtered off, and to the filtrate was added 140 ml of 5% hydrochloric acid. The precipitate was collected by filtration and sufficiently washed with water. The resulting crude product was recrystallized from ethanol to obtain 30.7 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05885990 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-6ca3338166144fbc994503deb3d92364 |
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| Source note | uspto-grants-1999_03 |
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