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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436607Generated: October 28, 2026

Acetone → HCID 12922310, compound

https://huagongshe.com/reaction/436607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantTolueneHCID 1140—
ReactantDimethyl SulfateHCID 6497—
Reactant4-Methoxy-1-methyl-3,5-diphenyl-1H-pyrazoleHCID 12498522—
ProductHCID 12922310HCID 12922310—

Reaction Conditions

Temperature130 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009277
Source datasetuspto-grants-1977_02
ORD IDord-fb97276136054b40a486c8a15c3bd6e0
Source noteuspto-grants-1977_02