Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 69861425 | HCID 69861425 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69861340 | HCID 69861340 | 31% |
Reaction Steps
To 160 mg of sodium hydroxide (60% oil dispersion) were added 30 ml of toluene and 1.00 g of 1-tert-butyl-4-(2,6-dichlorophenyl)-5-amino-pyrazolin-3-one, and the mixture was heated for 2 hours at 100° C. To this was added 550 ml of isopropyl mathanesulfonate, and the mixture was heated for additional 3 hours at 100° C. After completion of the reaction, water was added, and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate anhydride, then, the solvent was distilled off under reduced pressure. The residue analyzed by 1H-NMR on the ratio of N-alkyl compound to O-alkyl compound being 31 to 69 was applied to column chromatography to obtain 353 mg (yield: 31%) of 1-tert-butyl-2-sec-butyl-4-(2,6-dichlorophenyl)-5-aminopyrazolin-3-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05869684 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-912a2e9dfdb748529b97494a61531dd8 |
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| Source note | uspto-grants-1999_02 |
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