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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494814생성일: 2026년 10월 26일

1-Methoxybuta-1,3-diene → 4-{2-[(e)-2-Methoxyethenyl]-2,3-dihydro-1-benzofuran-5-yl}benzonitrile

https://huagongshe.com/reaction/494814

반응식

참여 물질

역할이름HCID투입량
반응물1-Methoxybuta-1,3-dieneHCID 18213—
반응물Sodium BicarbonateHCID 516892—
반응물4-(4-Hydroxy-3-iodophenyl)benzonitrileHCID 10358676—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4-{2-[(e)-2-Methoxyethenyl]-2,3-dihydro-1-benzofuran-5-yl}benzonitrileHCID 22274603549.9%

반응 조건

온도23 °C

반응 단계

A solution of Example 1A (0.20 g, 0.623 mmol), 1-methoxybutadiene (0.18 g, 2.18 mmol), palladium diacetate (0.007 g, 0.031 mmol), sodium bicarbonate (0.261 g, 3.11 mmol) and tetrabutyl ammonium chloride (0.173 g, 0.623 mmol) was heated at 60° C. in DMF (3 mL) under an atmosphere of nitrogen for 36 hours. The reaction was cooled to 23° C., diluted with CH2Cl2 (50 mL), filtered through Celite. The solution was concentrated under reduce pressure and the residue was purified on silica using CH2Cl2 to give the titled compound (0.95 g, 55%). 1HNMR (CDCl3): 3.05 (m, 1H), 3.40 (m, 1H), 3.60 (s, 3H), 5.00 (m, 1H), 5.22 (m, 1H), 6.72 (d, J=14 Hz, 1H), 6.83 (d, J=7 Hz, 1H), 7.38 (m, 2H), 7.65 (m, 4H); MS (DCI): 278 (M+H+), 295 (M+NH4+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538138B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-4ff6943717344cc6a31885b631682cf6
출처 메모uspto-grants-2009_05