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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22930생성일: 2026년 10월 23일

Acetic Acid → Methyl-(2E)-2-cyano-3-(2,3-dihydro-1-benzofuran-5-yl)-2-butenoate

https://huagongshe.com/ko/reaction/22930

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물BenzylamineHCID 7504—
반응물Methyl cyanoacetateHCID 7747—
반응물1-(2,3-Dihydro-5-benzofuranyl)ethanoneHCID 145220—
용매TolueneHCID 1140—
생성물Methyl-(2E)-2-cyano-3-(2,3-dihydro-1-benzofuran-5-yl)-2-butenoateHCID 6974677460.1%

반응 단계

To a stirred solution of 5-acetyl-2,3-dihydrobenzo[b]furan (Aldrich) (1 g, 6.17 mmol) in toluene (60 ml) was added methyl cyanoacetate (0.60 ml, 6.78 mmol), benzylamine (0.07 ml, 0.61 mmol) and acetic acid (0.3 ml, 5.3 mmol) and the whole refluxed in a Dean-Stark apparatus for 16 h. The reaction mixture was cooled, washed with 2N HCl (30 ml), NaHCO3 (30 ml), brine (30 ml), dried (MgSO4) and evaporated to a yellow residue. This residue was purified by column chromatography using 15-20% EtOAc in pentane as eluant to provide the title product (902 mg, 60%); 1HNMR (400 MHz, CDCl3) δ: 2.65 (s, 3H), 3.25 (t, 2H), 3.9 (s, 3H), 4.6 (t, 2H), 6.8 (d, 1H), 7.25 (d, 1H), 7.8 (s, 1H); LRMS: M+NH4+, 261. (ES+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849649B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-8e35362516b442d983fbea020c66b3ad
출처 메모uspto-grants-2005_02