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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519960Generated: November 3, 2026

4-Methylpyrazole → HCID 68787041, compound

https://huagongshe.com/reaction/1519960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpyrazoleHCID 3406—
Reactant2-Chloro-3-nitrothiopheneHCID 220186—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68787041HCID 68787041—

Reaction Steps

Potassium tert-butoxide (2.78 g, 24.8 mmol) and 4-methyl-1H-pyrazole (3.0 ml g, 37.3 mmol) in DMF (50 ml) was stirred for 30 min. 2-chloro-3-nitrothiophene (3.08 g, 18.7 mmol) was added and the solution was placed into a preheated oil bath at 100° C. After stirring for 1 h, the solution was diluted with brine and extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was flash chromatographed with 9:1, 4:1, 7:3, 3:2, and 1:1 hexane:ethyl acetate as the eluant to yield 4-methyl-1-(3-nitrothiophen-2-yl)-1H-pyrazole. Method [1] Retention time 1.80 min by HPLC (MH+ 210).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073891B2
Source datasetuspto-grants-2015_07
ORD IDord-3dbfd5cb60f3481999db517ab9a0d3a9
Source noteuspto-grants-2015_07