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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132055생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/132055

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물2-Benzylidene-but-3-ynenitrileHCID 86030656—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Phenyl-5-(trimethylsilyl)-1H-pyrazole-3-carbonitrileHCID 1314478969.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07385059B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-0f08b5cbfbd34341958661ce7d83229f
출처 메모uspto-grants-2008_06