Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 4-Methoxy-1-methyl-3,5-diphenyl-1H-pyrazole | HCID 12498522 | — |
| Product | HCID 12922310 | HCID 12922310 | — |
Reaction Steps
4-Methoxy-1-methyl-3,5-diphenylpyrazole (20 g, 0.076 mole) is suspended in dimethyl sulfate (23 g) at 20° C and the mixture is stirred and the reaction temperature raised to 130° C. At 70° C the mixture becomes a homogeneous solution and at 130° C some darkening occurs. After maintaining the reaction at 130° C for 1 hour, it is cooled and the mixture poured into toluene (250 ml). The toluene layer is decanted off and further toluene is added, decanted off, and this sequence repeated a third time. The residual oil, obtained from the above treatment, is then treated with acetone (10 ml) which has been dried over anhydrous potassium carbonate. This yields a crystalline product which is filtered off and washed with ether. The acetone filtrate is evaporated to give 27.5 g of oil, dissolved in water, and extracted with chloroform. The chloroform layer is evaporated to a small volume and then ether added. A white precipitate is obtained; combined yield 22 g (74%) of melting point 104.5°-105° C is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04009277 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-fb97276136054b40a486c8a15c3bd6e0 |
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| Source note | uspto-grants-1977_02 |
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