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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29286생성일: 2026년 10월 24일

Triethylamine → 4-(3-Methoxy-prop-1-ynyl)-3-methyl-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/29286

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-MethoxypropyneHCID 69393—
반응물Ethyl acetate hexaneHCID 21226206—
반응물3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl esterHCID 86599026—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물4-(3-Methoxy-prop-1-ynyl)-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 6871294753%

반응 조건

온도90 °C

반응 단계

To the product of Example 20, Step 1, 3-methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid ethyl ester (860 mg, 2.4 mmol, 1 eq), in 7 mL of DMF under nitrogen was added 98 mg of PdCl2(PPh3)2 (0.14 mmol, 0.06 eq), 0.42 mL of 3-methoxy-propyne (5.0 mmol, 2.1 eq) and 1.36 mL of triethylamine (9.7 mmol, 4.0 eq). The reaction mixture was heated to 90° C. for 18 h. After work up and column chromatography (4% ethyl acetate/hexane), 4-(3-methoxy-prop-1-ynyl)-3-methyl-benzofuran-2-carboxylic acid ethyl ester was obtained in 53% yield (343 mg). 1H NMR (400 MHz, CDCl3) δ ppm 1.4 (t, J=7.2 Hz, 3 H) 2.8 (t, 3 H) 3.5 (s, 3 H) 4.4 (s, 2 H) 4.5 (q, J=7.2 Hz, 2 H) 7.4 (m, 2 H) 7.5 (dd, J=7.7, 1.6 Hz, 1 H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0ac7317bcc5943bca318ec231f53062c
출처 메모uspto-grants-2008_09