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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30285생성일: 2026년 10월 24일

18-Crown-6 → 3-Thiophen-3-yl-acrylic acid ethyl ester

https://huagongshe.com/ko/reaction/30285

반응식

참여 물질

역할이름HCID투입량
반응물18-Crown-6HCID 28557—
반응물3-ThiophenecarboxaldehydeHCID 68135—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물Ethyl [bis(2,2,2-trifluoroethoxy)phosphinyl]acetateHCID 11759356—
용매TetrahydrofuranHCID 8028—
생성물3-Thiophen-3-yl-acrylic acid ethyl esterHCID 6691475382.7%

반응 단계

Potassium bis(trimethylsilyl)amide (3.92 g, 19.7 mol) was added to a solution of 18-Crown-6 (9.95 g, 37.6 mmol) and [Bis-(2,2,2 trifluoro-ethoxy)-phosphoryl]-acetic acid ethyl ester (6.54 g, 19.7 mmol) in dry THF (200 mL) at −78° C. After 30 minutes of stirring at this temperature, thiophene-3-carbaldehyde (2.0 g, 19.7 mmol) was added and the reaction was stirred for 3 hours at −780C after which the reaction was quenched with saturated ammonium chloride (200 mL). The reaction mixture was allowed to come to room temperature and was extracted with ethyl acetate (3×250 mL) and the combined organic extracts were washed with 10% HCl (200 mL), brine (200 mL) and dried with MgSO4 Evaporation of the solvent in vacuo gave the crude product that was purified by silica-gel chromatography using a 0-40% ethylacetate-hexane gradient to afford the subtitle compound (2.7 g, 82.7%). MS calculated for C9H10O2S+H: 183, observed: 183; 1H NMR (300 MHz, CDCl3, ppm) 1.31 (t, J=7 Hz, 3H); 4.22 (q, J=7 Hz, 2H); 5.83 (d, J=13 Hz, 1H); 6.87 (d, J=7 Hz, 1H); 7.24-7.28 (m, 1H); 7.54 (dd, J1=5 Hz, J2=1 Hz, 1H); 8.07 (br d, J=3 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423056B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ac12fa240ab84c8694e525d002c85c2e
출처 메모uspto-grants-2008_09