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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490765생성일: 2026년 10월 25일

Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → Methyl 2-(6-hydroxy-1-benzofuran-3-yl)acetate

https://huagongshe.com/reaction/490765

반응식

참여 물질

역할이름HCID투입량
반응물Acetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
반응물6-Hydroxy-3-coumaranoneHCID 235717—
생성물Methyl 2-(6-hydroxy-1-benzofuran-3-yl)acetateHCID 20770861—

반응 단계

A mixture of 6-hydroxy-(2H)-benzofuran-3-one (5.0 g, 33.3 mmol), methyl (triphenylphosphoranylidene)acetate (25.0 g, 73 mmol), and xylenes (100 mL) is refluxed 6 hr. The reaction is concentrated and diluted with enough 1M aqueous hydrochloric acid to adjust pH to 2-3. The product is extracted into ethyl acetate (3×100 mL). The combined extracts are dried over anhydrous magnesium sulfate, filtered and concentrated. The residue is purified via silica chromatography eluting with 7:3 hexanes:ethyl acetate to afford the product as a orange oil, 1.3 g, 20%. MS M++1 207. The structure is confirmed by 1H NMR spectroscopy.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528160B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-2e9f6240f632462d98765b5979e85e6b
출처 메모uspto-grants-2009_05