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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551917생성일: 2026년 10월 27일

Acetone → 2,2-dimethyl-4-oxo-4H-1,3-benzodioxine-6-carboxylic acid

https://huagongshe.com/reaction/551917

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물4-Hydroxyisophthalic acidHCID 12490—
용매Trifluoroacetic acidHCID 6422—
용매Trifluoroacetic anhydrideHCID 9845—
생성물2,2-dimethyl-4-oxo-4H-1,3-benzodioxine-6-carboxylic acidHCID 5755448977%

반응 조건

온도100 °C

반응 단계

A suspension of 4-hydroxyisophtalic acid (Aldrich, 5.0 g, 27.5 mmol) in acetone (10 mL), TFA (30 mL) and TFAA (10 mL) was heated at 100° C. for 24 hrs. The reaction mixture was concentrated under reduced pressure. The residue was taken up with an aqueous solution of HCl (100 mL, 1N) and extracted with EtOAc (3×200 L); The combined organic layers were dried over MgSO4 and the solvents were removed under reduced: pressure. The crude compound was recrystallized in Et2O (50 mL) to give 4.67 g (77%) of the title compound as a beige powder. 1H NMR (DMSO-d6) δ: 8.37 (d J=1.9 Hz, 1H), 8.19 (dd, J=2.2 and 8.7 Hz, 1H), 7.23 (d, J=8.3 Hz, 1H), 1.72 (s, 6H). HPLC, Rt: 2.40 min (purity: 95.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947851B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-5239bc217de14bc19f5e1c209b28bbc8
출처 메모uspto-grants-2011_05