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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29290생성일: 2026년 10월 23일

Nitroethane → 3-Methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/29290

반응식

참여 물질

역할이름HCID투입량
반응물NitroethaneHCID 6587—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물4-Ethynyl-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 86058915—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매AcetonitrileHCID 6342—
생성물3-Methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl esterHCID 6871470725%

반응 단계

To a solution of 4-ethynyl-3-methyl-benzofuran-2-carboxylic acid ethyl ester (228 mg, 0.99 mmol, 1 eq.) in acetonitrile (5 mL) under argon, was added di-tert-butyl dicarbonate (327 mg, 1.5 mmol, 1.5 eq.), and 4-(dimethylamino)pyridine (12 mg, 0.1 mmol, 0.1 eq.). Nitroethane (79 uL, 1.1 mmol, and 1.1 eq.) in acetonitrile (5 mL) was added drop-wise to the reaction mixture, and the reaction was stirred at room temperature for 72 hours. After work-up and flash column chromatography, 3-methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl ester was obtained in 25% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.4 (t, J=7.1 Hz, 3 H) 2.3 (s, 3 H) 2.4 (s, 3 H) 4.4 (q, J=7.1 Hz, 2 H) 6.8 (s, 1 H) 7.5 (dd, J=7.5, 0.9 Hz, 1 H) 7.6 (m, 1 H) 7.9 (dd, J=8.5, 0.9 Hz, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-3f44d056d2ef4778a58629bd5e844bbb
출처 메모uspto-grants-2008_09