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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655181Generated: November 3, 2026

Acetone → HCID 67855017, compound

https://huagongshe.com/reaction/1655181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 54321359HCID 54321359—
ProductHCID 67855017HCID 67855017—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 0.4 gram (0.001 mole) of 3-[4-cyano-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazol-5-yl]acrylic acid in 25 mL of acetone were added in succession 0.2 gram (0.001 mole) of potassium carbonate and 0.2 gram (0.001 mole) of 1,1-dimethylethyl bromoacetate. Upon completion of the addition, the reaction mixture was stirred at 25° C. for 25 minutes, and then it was heated to reflux where it was stirred for one hour. After this time, the reaction mixture was cooled and concentrated under reduced pressure to a residue. The residue was shaken with methylene chloride and water. The organic layer was washed with water and then dried with calcium sulfate. The mixture was filtered through silica gel. The silica gel filter pad was washed with petroleum ether. The combined filtrates were concentrated under reduced pressure, yielding 0.5 gram of 1,1-dimethylethoxycarbonylmethyl 3-[4-cyano-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazol-5-yl]acrylate; m.p. 110° -112° C. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250504
Source datasetuspto-grants-1993_10
ORD IDord-52892f82830043959792664db182b51c
Source noteuspto-grants-1993_10