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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 577560Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/577560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dihydroxybenzoic AcidHCID 19—
EduktAcetoneHCID 180—
EduktTrifluoroacetic anhydrideHCID 9845—
LösungsmittelTrifluoroacetic acidHCID 6422—
Produkt8-hydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-oneHCID 2255699534%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040515B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-c2b41c88835c4a1980df45f7d1297050
Quellennotizuspto-grants-2015_05