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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 495180생성일: 2026년 10월 25일

Acetic Acid → Methyl 2-acetyl-3,5-diallyloxyphenylacetate

https://huagongshe.com/reaction/495180

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 3,5-diallyloxyphenylacetateHCID 23116191—
용매Trifluoroacetic acidHCID 6422—
생성물Methyl 2-acetyl-3,5-diallyloxyphenylacetateHCID 6842177670.4%

반응 조건

온도4 °C

반응 단계

Methyl 3,5-diallyloxyphenylacetate (40 g, 0.14 mol) obtained in Example 5, Step 1 was dissolved in trifluoroacetic acid (0.15 L). After the solution was cooled to 4° C., acetic acid (9.5 mL, 0.17 mol) and trifluoroacetic anhydride (40 mL, 0.28 mol) were added thereto, followed by stirring at 4° C. for 3.5 hours. The reaction mixture was gradually added to a saturated aqueous solution of sodium hydrogencarbonate for neutralization, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/20-1/6) to obtain methyl 2-acetyl-3,5-diallyloxyphenylacetate (30 g, 65%). 1H-NMR (CDCl3, 300 MHz) δ (ppm): 6.43 (d, J=2.2 Hz, 1H), 6.37 (d, J=2.2 Hz, 1H), 6.07-5.98 (m, 2H), 5.44-5.27 (m, 4H), 4.57-4.52 (m, 4H), 3.69 (s, 2H), 3.68 (s, 3H), 2.53 (s, 3H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538224B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-d7b2a0324f5548dfb1e51811df6fdf0b
출처 메모uspto-grants-2009_05