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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 577560생성일: 2026년 10월 26일

2,3-Dihydroxybenzoic Acid → 8-hydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one

https://huagongshe.com/reaction/577560

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dihydroxybenzoic AcidHCID 19—
반응물AcetoneHCID 180—
반응물Trifluoroacetic anhydrideHCID 9845—
용매Trifluoroacetic acidHCID 6422—
생성물8-hydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-oneHCID 2255699534%

반응 단계

Trifluoroacetic acid anhydride (42.0 mL, 300 mmol) was added dropwise to a cooled (−5° C.) solution of 2,3-dihydroxybenzoic acid (8.30 g, 53.9 mmol) in trifluoroacetic acid (83 mL), with stirring. Acetone (14.0 mL, 190 mmol) was then added dropwise over 27 minutes, and the mixture stirred and allowed to warm gradually to room temperature over 16.5 hours. The volatiles were concentrated under vacuum, the residue was dissolved in ethyl acetate (100 mL), and the solution slowly added to a rapidly stirred saturated aqueous sodium bicarbonate solution (200 mL). After gas evolution ceased, the mixture was extracted with ethyl acetate (3×100 mL). The combined organic extracts were dried over magnesium sulfate, filtered, concentrated, and purified by silica gel chromatography (ethyl acetate/heptane) to give 8-hydroxy-2,2-dimethyl-4H-1,3-benzodioxin-4-one (123a, 3.55 g, 34% yield) as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040515B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-c2b41c88835c4a1980df45f7d1297050
출처 메모uspto-grants-2015_05