Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Reactant | HCID 13343756 | HCID 13343756 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178429018 | HCID 178429018 | 78.9% |
Reaction Steps
20 ml of water and 17.0 g of purified potassium ethylxanthate were added to 20.0 g of 5,6-diamino-1,1,3,3-tetramethyl-2-indanone, dissolved in 200 ml of alcohol, in a 750 ml sulfonation flask equipped with stirrer, thermometer, reflux condenser. The mixture was left to boil at reflux overnight, then diluted with 200 ml of water, neutralized with 20 ml of glacial acetic acid and stirrer at 60°-70° C. for an additional 1 hour. After cooling to 20° C., were removed by filtration under suction. There were obtained 18.8 g (78.9% of theory) of 5,7-dihydro-2-mercapto-5,5,7,7-tetramethylindeno(5,6-d)-imidazol-6(1H)-one with a melting point above 300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04599347 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-0e702c4567a4422089032c1bfa673b93 |
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| Source note | uspto-grants-1986_07 |
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