Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Ethaneperoxoic acid, mixt. with acetic acid | HCID 197110 | — |
| Reactant | HCID 178463108 | HCID 178463108 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178463106 | HCID 178463106 | 77% |
Reaction Steps
0.39 Gram (1.2 mmol) of 6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonyl-5,8-dimethylthiochrom-2-en-4-one was dissolved in 4 ml of chloroform, and 0.62 g (2.6 mmol) of a 32 wt % peracetic acid/acetic acid solution was added. The mixture was allowed to react at room temperature for 5 hours, and then allowed to react at 50° C. for 2 hours and further stirred at room temperature for 17 hours. After the reaction, the reaction mixture was diluted with water, and a 1 wt % sodium sulfite aqueous solution was added to decompose excess peracetic acid. An organic substance was extracted with ethyl acetate, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to give 0.33 g (yield 77%) of the titled compound. Table 24 shows the physical property data of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06159904 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-02f82193500049619f4f1911fc9938c0 |
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| Source note | uspto-grants-2000_12 |
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