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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1719656Erstellt: 25. Oktober 2026

Methane → HCID 70093312, Verbindung

https://huagongshe.com/reaction/1719656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktOxygenHCID 977—
EduktBenzyltrimethylammonium hydroxideHCID 66854—
Edukt2-FluorofluoreneHCID 241132—
LösungsmittelPyridineHCID 1049—
ProduktHCID 70093312HCID 70093312—

Reaktionsschritte

2-Fluorofluorene (824.7 g, 4.48 mol) was dissolved in pyridine (4 L) and stirred. A 40% solution of Triton B (100 mL of benzyltrimethylammonium hydroxide 40% in pyridine according to a general procedure of U. Sprinzak, J. Amer. Chem. Soc. 80 (1958) 5449) was added and oxygen was bubbled into the vigorously stirred solution. This exothermic reaction was run for 20 hours whereupon an additional portion of the Triton B solution (50 mL) was added with continued stirring and oxygen addition for an additional 24 hours. The resulting dark green reaction mixture was treated with Norite (100 g, neutralized charcoal), stirred for 30 minutes and filtered through a Celite pad (diatomaceous earth filter aid). The filter pad was then washed with pyridine (1 L). The combined filtrates were concentrated to a small volume in vacuo with heat. A 5% solution of hydrochloric acid in water (1 L) was added and the pyridine was azeotrophed in vacuo with heat. This process was repeated until a total of 6-8 L of water were evaporated. The granular product was filtered and washed with water (4 L) and air dried. The yellow-orange product was melted and distilled through a large bore short path distillation apparatus (bp 167°-170° C.; 1.5 mm Hg) to yield into a chilled receiving flask the bright yellow 2-fluorofluorenone (600 g) with a m.p. 113°-115° C. and m/e+. 198 for C13H7FO.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04540700
Quelldatensatzuspto-grants-1985_09
ORD IDord-232be3fab321458bbcdaa902d9ffed98
Quellennotizuspto-grants-1985_09