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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | ((1,1-Dimethyl-2-propynyl)oxy)trimethylsilane | HCID 87344 | — |
| 반응물 | 3-cyano-N,4-dimethoxy-N-methylbenzamide | HCID 59354763 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Methoxy-5-(4-methyl-4-(trimethylsilyloxy)pent-2-ynoyl)benzonitrile | HCID 59354821 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08933074B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-6427279982f54fa1addb21f06a5a3c4b |
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| 출처 메모 | uspto-grants-2015_01 |
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