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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276027Generated: October 31, 2026

Methylhydrazine → ethyl 5-(2,6-difluorophenyl)-1-methyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/2276027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantDiethyl OxalateHCID 7268—
Reactant1-(2,6-Difluorophenyl)ethan-1-oneHCID 83643—
ReactantSodium t-butoxideHCID 23676156—
SolventEthanolHCID 702—
Productethyl 5-(2,6-difluorophenyl)-1-methyl-1H-pyrazole-3-carboxylateHCID 6661394012.5%

Reaction Steps

To a mixture of 2,6-difluoroacetophenone (4.7 g, 0.03 mol) and 1,2-diethyl ethanedioate (4.8 g, 0.033 mol) in ethanol (33 mL) was added sodium tert-butoxide (3.17 g, 0.033 mol). After 1 h, more ethanol (30 mL) was added to the reaction mixture and stirring was continued for 1 h. The reaction mixture was partitioned between hydrochloric acid (1 N) and diethyl ether. The organic phase was separated, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to half its original volume. To the resulting mixture was added methylhydrazine (1.52 g, 0.033 mol) and stirring was continued overnight. The reaction mixture was concentrated under reduced pressure and the resulting material was purified by silica gel chromatography (5 to 20% gradient of ethyl acetate in methylene chloride as eluant) to provide the title compound as a solid (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09131693B2
Source datasetuspto-grants-2015_09
ORD IDord-f8f72453370d49dfa74ee29099e3ae23
Source noteuspto-grants-2015_09