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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1425870생성일: 2026년 10월 26일

((1,1-Dimethyl-2-propynyl)oxy)trimethylsilane → 2-Methoxy-5-(4-methyl-4-(trimethylsilyloxy)pent-2-ynoyl)benzonitrile

https://huagongshe.com/reaction/1425870

반응식

참여 물질

역할이름HCID투입량
반응물((1,1-Dimethyl-2-propynyl)oxy)trimethylsilaneHCID 87344—
반응물3-cyano-N,4-dimethoxy-N-methylbenzamideHCID 59354763—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-Methoxy-5-(4-methyl-4-(trimethylsilyloxy)pent-2-ynoyl)benzonitrileHCID 5935482156%

반응 조건

온도-78 °C

반응 단계

To a −78° C. stirred solution of trimethyl(2-methylbut-3-yn-2-yloxy)silane (1.9 g, 12.501 mmol) in dry THF (25 mL), n-BuLi (2.80 mL, 4.50 mmol, 1.6 M in hexane) was added dropwise over 10 minutes under an inert atmosphere. The reaction was stirred for 30 min at −78° C., and then a solution of 3-cyano-N,4-dimethoxy-N-methylbenzamide (1.10 g, 5.01 mmol) in dry THF (10 mL) was added to reaction mixture and stirring was continued for an additional 3 h at −78° C. The reaction mixture was quenched with a saturated NH4Cl solution and extracted with EtOAc (2×50 mL). The combined organic layers were washed with water (20 mL) and brine (20 mL), dried over Na2SO4, filtered and concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography eluting with 5% EtOAc in hexanes to afford 2-methoxy-5-(4-methyl-4-(trimethylsilyloxy)pent-2-ynoyl)benzonitrile (0.8 g, 56%) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933074B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-6427279982f54fa1addb21f06a5a3c4b
출처 메모uspto-grants-2015_01