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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854991생성일: 2026년 10월 27일

Ethynyltributyltin → ethyl 8-chloro-6-ethynyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854991

반응식

참여 물질

역할이름HCID투입량
반응물EthynyltributyltinHCID 621176—
반응물ethyl 8-chloro-6-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 58934641—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물ethyl 8-chloro-6-ethynyl-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 8659947775.6%

반응 단계

To 0.86 g (2.0 mmole) of ethyl 8-chloro-6-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylate was added 46 mg (0.040 mmole) tetrakis(triphenylphosphine)palladium(0), 6 mLs degassed toluene and 0.64 mL (0.69 g, 2.2 mmole) tributyl(ethynyl)tin. The stirred mixture was heated to reflux for 3 h. After allowing the reaction to cool, the mixture was washed with 20% aq. ammonium fluoride and the aqueous layer extracted three times with diethyl ether. The combined extracts were filtered through silica, the silica washed with diethyl ether and the organic fractions concd in vacuo. Chromatographic purification (70 g silica, 5% ethyl acetate/hexanes) afforded a solid which was triturated with hexanes to give 0.50 g (75.6%) of a crystalline solid: 1H NMR (d6-acetone/400 MHz) 1.32 (t, 3H, J=7.1 Hz), 3.73 (s,1H), 4.32 (m, 2H), 6.04 (q, 1H, J=6.9 Hz), 7.60 (m, 2H), 7.90 (s, 1H); 19F NMR (d6-acetone/400 MHz) −79.6 (d, 3F, J=6.8 Hz); MS(ESI+) 331 (M+1, 100, one Cl pattern).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259266B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-d7d523f59f574524b6429c23318514cc
출처 메모uspto-grants-2007_08