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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29457생성일: 2026년 10월 24일

3-Methyl-1-benzofuran-2-carboxylic acid → 3-Methyl-2-benzofuranmethanol

https://huagongshe.com/ko/reaction/29457

반응식

참여 물질

역할이름HCID투입량
반응물3-Methyl-1-benzofuran-2-carboxylic acidHCID 600591—
반응물Borane;tetrahydrofuranHCID 2723981—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-Methyl-2-benzofuranmethanolHCID 1024110887%

반응 단계

A solution of 3-methyl-benzofuran-2-carboxylic acid (2.0 g, 11.4 mmol, 1 eq) in 60 mL of THF under nitrogen was placed in water bath. Then 30 mL of BH3.THF (1.0 M in THF, 30 mmol, 2.6 eq) was added dropwise. The reaction mixture was allowed to stir at room temperature for 12 h. Then the reaction was quenched with methanol (10 mL). Solvent was removed in vacuo and the residue was subjected to column chromatography eluting with 20% ethyl acetate/hexane to give (3-methyl-benzofuran-2-yl)-methanol (1.6 g) in 87% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.2 (s, 3 H) 4.5 (d, J=5.8 Hz, 2 H) 5.3 (t, J=5.8 Hz, 1 H) 7.3 (m, 2 H) 7.5 (m, 1 H) 7.6 (m, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5d8efb45f78b407db502724f69cc21b4
출처 메모uspto-grants-2008_09