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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674483Generated: October 30, 2026

Hydrochloric Acid → HCID 67339313, compound

https://huagongshe.com/reaction/1674483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantMethylhydrazineHCID 6061—
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
SolventEthanolHCID 702—
ProductHCID 67339313HCID 6733931361.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 4,4,4-trifluoroacetoacetate (120 g, 0.65 mol) was dissolved in 650 ml of ethanol and the solution was cooled down to 0° C. A 37% aqueous solution of formaldehyde (53 g, 0.65 mol) was added and the mixture was stirred for 15 minutes at 0° C. Methylhydrazine (30 g, 0.65 mol) was added and the reaction mixture was heated to reflux. After reaching the reflux temperature, 2.5 ml of concentrated hydrochloric acid were added, and refluxing was continued for 16 h. Subsequently, the mixture was cooled down and the solvent was removed in vacuo. The remainder was taken up in water and extracted with ethyl acetate. The combined organic layer was washed with water, dried over magnesium sulfate and evaporated. The remaining oil was purified by silica gel chromatography using ethyl acetate and hexane as eluents, yielding 90 g of 1-methyl-3-trifluoromethyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003626B2
Source datasetuspto-grants-2011_08
ORD IDord-2f00229a16c34712b4aea5238a6b1061
Source noteuspto-grants-2011_08