돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69322생성일: 2026년 10월 23일

Isopropenyl acetate → 1-(4-Methoxy-2-methylphenyl)-2-propanone

https://huagongshe.com/ko/reaction/69322

반응식

참여 물질

역할이름HCID투입량
반응물Isopropenyl acetateHCID 7916—
반응물Tri-o-tolylphosphineHCID 80271—
반응물1-Bromo-4-methoxy-2-methylbenzeneHCID 117915—
반응물Potassium FluorideHCID 522689—
반응물Tributyltin methoxideHCID 16683411—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물1-(4-Methoxy-2-methylphenyl)-2-propanoneHCID 24721492—

반응 단계

Four batches of this experiment were carried out (4×250 g substrate). Tributyl(methoxy)stannane (400 g, 1.24 mol), 1-bromo-4-methoxy-2-methylbenzene (250 g, 1.24 mol), prop-1-en-2-yl acetate (187 g, 1.87 mol), palladium(II) acetate (7.5 g, 33 mmol) and tris(2-methylphenyl)phosphane (10 g, 33 mmol) were stirred together in toluene (2 L) at 100° C. for 18 hours. After cooling to room temperature, the reaction mixture was treated with aqueous potassium fluoride solution (4 M, 400 mL) and stirred for 2 hours at 40° C. The resulting mixture was diluted with toluene (500 mL) and filtered through Celite; the filter pad was thoroughly washed with ethyl acetate (2×1.5 L). The organic phase from the combined filtrates was dried over sodium sulfate, filtered, and concentrated in vacuo. Purification via silica gel chromatography (Gradient: 0% to 5% ethyl acetate in petroleum ether) provided the product as a yellow oil. Combined yield: 602 g, 3.38 mol, 68%. LCMS m/z 179.0 [M+H+]. 1H NMR (400 MHz, CDCl3) δ 7.05 (d, J=8.3 Hz, 1H), 6.70-6.77 (m, 2H), 3.79 (s, 3H), 3.65 (s, 2H), 2.22 (s, 3H), 2.14 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822494B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-26c3853413ed4f609f020779bb13ff9a
출처 메모uspto-grants-2014_09