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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75244생성일: 2026년 10월 25일

Trimethylsilylacetylene → HCID 21930937, 화합물

https://huagongshe.com/reaction/75244

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참여 물질

역할이름HCID투입량
반응물TrimethylsilylacetyleneHCID 66111—
반응물HCID 21930956HCID 21930956—
촉매Palladium(2+) acetate--triphenylphosphane (1/2/2)HCID 84538—
용매TolueneHCID 1140—
생성물HCID 21930937HCID 2193093793%

반응 단계

A mixture of bromide 5 (0.3 g, 0.73 mmol), trimethylsilylacetylene (0.143 g, 1.46 mmol) and bis(triphenylphosphine)-palladium-(II) acetate (55 mg, 0.073 mmol) in a mixed solvent system of toluene (20 mL) and anhydrous TEA (50 mL) was heated to reflux under argon. After stirring for 12 hours at reflux, the mixture was cooled to room temperature and the precipitate which formed was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was treated with a saturated aqueous solution of NaHCO3 (20 mL), and extracted with CHCl3 (3×25 mL). The combined extracts were washed with brine and dried (Na2SO4). After removal of solvent under reduced pressure, the residue was purified by flash chromatography (silica gel, EtOAc) to afford 6 (XLiXHeII-048) as a white solid (0.29 g, 93%). This benzodiazepine can also be obtained from 2 in 45% yield by following the same procedure 6 (XLiXHeII-048): mp: 170-172° C.; IR (KBr) 2958, 2152, 1718 cm−1; 1H NMR (CDCl3) δ 0.23 (s, 9H), 1.42 (t, 3H, J=7.2 Hz), 4.04 (d, 1H, J=12.6 Hz), 4.41 (m, 2H, J=7.2 Hz), 6.23 (d, 1H, J=12.6 Hz), 7.35-7.55 (m, 7H), 7.73 (dd, 1H, J=8.3 Hz, J=1.9 Hz), 7.93 (s, 1H); MS (EI) m/e (relative intensity) 427 (M+, 76), 412 (5), 381 (55), 353 (100) 303 (10), 287 (7). Anal. Calcd. for C25H25N3O2Si.1/3 EtOAc: C, 69.22; H, 6.01; N, 9.20. Found: C, 68.87; H, 5.81; N, 9.37.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835424B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1c80403410ea49b793bd2d64dc4ecc39
출처 메모uspto-grants-2014_09