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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222461생성일: 2026년 10월 26일

Toluene → (6-Acetoxymethyl-benzofuran-3-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/222461

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Carboxymethylene triphenylphosphoraneHCID 10870911—
반응물Acetic acid 3-oxo-2,3-dihydro-benzofuran-6-ylmethyl esterHCID 68526065—
생성물(6-Acetoxymethyl-benzofuran-3-yl)-acetic acid ethyl esterHCID 68523733—

반응 단계

To a solution of acetic acid 3-oxo-2,3-dihydro-benzofuran-6-ylmethyl ester (1.50 g, 7.27 mmol) in toluene (260 mL) was added (caboxymethylene)triphenyl phosphorane (12.67 g, 36.37 mmol) and the mixture was refluxed for 24 h. The reaction mixture was allowed to cool to room temperature and concentrated. The residue was purified by column chromatography (ethylacetate:hexane; 5:95) to give the (6-acetoxymethyl-benzofuran-3-yl)-acetic acid ethyl ester as a off white solid (1.15 g, 57%). 1H NMR (CDCl3, 400 MHz) 1.27 (t, J=7.1 Hz, 3H), 2.11 (s, 3H), 3.69 (s, 2H), 4.19 (q, J=7.1 Hz, 2H), 5.21 (s, 2H), 7.26 (d, J=8.0 Hz, 1H), 7.50 (s, 1H), 7.56 (d, J=8.0 Hz, 1H), 7.65 (s, 1H), 13C NMR (CDCl3, 100 MHz) 14.2, 21.0, 29.9, 61.1, 66.4, 111.6, 113.1, 119.8, 123.1, 127.7, 132.6, 143.5, 155.2, 170.5, 170.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207216B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-e0c8d50cc63d4ad6bd10457de82110bb
출처 메모uspto-grants-2012_06