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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22925생성일: 2026년 10월 24일

Ethyl Acetate → 2,3-Dihydro-1-benzofuran-7-carbaldehyde

https://huagongshe.com/ko/reaction/22925

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물DihydrobenzofuranHCID 10329—
반응물Methane, dichloromethoxy-HCID 21004—
반응물Tin tetrachlorideHCID 24287—
용매DichloromethaneHCID 6344—
용매PentaneHCID 8003—
생성물2,3-Dihydro-1-benzofuran-7-carbaldehydeHCID 27950180.6%

반응 조건

온도0 °C

반응 단계

2,3-Dihydrobenzo[b]furan (Maybridge Chemicals) (25 g, 0.21 mole) was taken up in DCM (500 ml) and stirred under nitrogen at 0° C. SnCl4 (36.5 ml, 0.3 mole) was added in one portion to produce a pale yellow solution. Dichloromethyl methyl ether (18.8 ml, 0.21 mole) was then added and the solution stirred for 30 min, after which time the cooling bath was removed and the reaction poured onto ice-water (1000 ml). The organic layer was separated, washed with water (2×100 ml), 2N HCl (100 ml) and brine (50 ml), and then charcoal (30 g) and Na2SO4 were added to the solution. Filtration through Celite and evaporation gave a black oil, which was subjected to flash chromatography using 7-10% EtOAc in pentane to give the title product (190 mg, 0.01%); 1HNMR (400 MHz, CDCl3) δ: 3.24 (t, 2H), 4.75 (t, 2H), 6.93 (t, 1H), 7.40 (d, 1H), 7.59 (d, 1H), 10.2 (s, 1H); LRMS: (M+H) 149, TS+. Anal. Found: C, 72.98; H, 5.46%. C9H8O2 requires C, 72.96; H, 5.44%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849649B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-ef796c20b36244388f7295ba69e44a8d
출처 메모uspto-grants-2005_02