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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 527657Erstellt: 24. Oktober 2026

Hydrogen Peroxide → 2,2-Difluoro-1,3-benzodioxol-4-ol

https://huagongshe.com/de/reaction/527657

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktTrimethyl borateHCID 8470—
EduktSodium HydroxideHCID 14798—
Edukt2,2-Difluoro-1,3-benzodioxoleHCID 74103—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelCyclohexaneHCID 8078—
Produkt2,2-Difluoro-1,3-benzodioxol-4-olHCID 1111654195,3%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

2,2-Difluoro-1,3-benzodioxole (320 mg, 2.05 mmol) was dissolved in THF (2.5 mL) and cyclohexane (1.2 mL) and the resulting solution cooled down to −78° C. sec-BuLi 2M solution in cyclohexane (1.025 ml, 2.05 mmol) was added drop wise and the reaction mixture stirred for 2 hours at −78° C. Trimethylborate (230 mg, 2.25 mmol) was added and the mixture was allowed to warm slowly to room temperature. A 30% w/w aqueous solution of H2O2 (4.1 mmol) and NaOH (82 mg, 2.05 mmol) were added and the reaction mixture stirred for 18 hours at room temperature. The reaction was quenched with a 2N aqueous solution of HCl and diluted with ethyl acetate. Two phases were separated and the organic layer was washed twice with brine, dried over Na2SO4 and evaporated to dryness, affording the title compound (340 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346790B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-83b7b301ea65407dbc620c3fc0d63a85
Quellennotizuspto-grants-2016_05