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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29311생성일: 2026년 10월 23일

3-Methyl-1-benzofuran-2-carboxylic acid → 3-Methyl-benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide

https://huagongshe.com/ko/reaction/29311

반응식

참여 물질

역할이름HCID투입량
반응물3-Methyl-1-benzofuran-2-carboxylic acidHCID 600591—
반응물4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
생성물3-Methyl-benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amideHCID 8659902755%

반응 단계

Amide coupling of 3-methyl-benzofuran-2-carboxylic acid with 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylamine was done according to Example 20, Step 4, to give 3-methyl-benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide in 55% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.3 (s, 12 H) 2.6 (s, 3 H) 7.4 (m, 1 H) 7.5 (m, 1 H) 7.7 (m, 3 H) 7.8 (d, J=7.3 Hz, 1 H) 7.9 (d, J=8.6 Hz, 2 H) 10.5 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-198390a6d33d4b68ad7a39f661b84849
출처 메모uspto-grants-2008_09