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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169921Generated: October 24, 2026

Trimethylsilyldiazomethane → 4-Phenyl-5-(trimethylsilyl)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/en/reaction/1169921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-Benzylidene-but-3-ynenitrileHCID 86030656—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-Phenyl-5-(trimethylsilyl)-1H-pyrazole-3-carbonitrileHCID 1314478969.1%

Reaction Steps

n-Butyl lithium (2.7 M solution in heptane) (3.3 ml, 9 mmol) was added drop wise to a stirred solution of trimethylsilyl diazomethane (2 M solution in diethyl ether) (4.5 ml, 9 mmol) in anhydrous THF (10 ml) at −78° C. under a nitrogen atmosphere, then stirred for a further 30 minutes. To this was added drop wise a solution of 2-benzylidene-but-3-yne nitrile (920 mg; 6 mmol) in anhydrous THF (5 ml), the mixture stirred for 30 minutes at −78° C. then gradually allowed to warm to room temperature overnight. The reaction mixture was diluted with ethyl acetate (30 ml) then washed with saturated ammonium chloride solution followed by brine. The ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated. The crude product was purified by flash column chromatography eluting with 1:8 then 1:4 ethyl acetate/hexane and the product containing fractions combined and evaporated to give 1.0 g of 4-phenyl-5-trimethylsilanyl-1H-pyrazole-3-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825140B2
Source datasetuspto-grants-2010_11
ORD IDord-0ec0cdbbe25b41109ce9e455177f71f9
Source noteuspto-grants-2010_11