Hydrochloric Acid → 9-Methylene-9H-fluorene

HRID 1275871

Reaktionsgleichung

Reaktionsgleichung von HRID 1275871
C(O[CH2:5][CH:6]1[C:18]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:12]2[C:7]1=[CH:8][CH:9]=[CH:10][CH:11]=2)(=O)C.CC(C)([O-])C.[K+].Cl>CCOCC>[CH2:5]=[C:6]1[C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:13]2[C:18]1=[CH:17][CH:16]=[CH:15][CH:14]=2

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 5401799-(Acetoxymethyl)fluoreneHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 781479-Methylene-9H-fluoreneAusbeute 94 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

A 1000 mL flask was charged with 9-acetoxymethylfluorene (30.0 g, 126 mmol) and anhydrous petroleum ether (bp 35-60° C., 400 mL, Aldrich) and it was cooled to 5° C. Solid potassium tert-butoxide (16.0 g, 142 mmol, Aldrich) was added in one portion. After stirring for 6 hours, the mixture was poured into dilute HCl (200 mL, 0.1 N). Et2O was added (100 mL); the layers were separated and the product extracted into Et2O (2×100 mL). Combined organic portions were dried over anhydrous MgSO4 and the solvent was removed via rotary evaporation. The crude product dibenzofulvene was isolated as a yellow solid (21.3 g, 94% yield, >99% pure by GC). Further purification was accomplished by recrystallization from petroleum ether, to yield dibenzofulvene in the form of white needles (Tm 51.5-53° C.).

Aufarbeitung

  1. customthe layers were separated
  2. extractionthe product extracted into Et2O (2×100 mL)
  3. dry with materialCombined organic portions were dried over anhydrous MgSO4
  4. customthe solvent was removed via rotary evaporation

Quellen und Nachweise

ORD-Eintrag
ord-54f4cf02a21b4680a27a9e5b6e869325
Quelldatensatz
uspto-grants-2000_12
Patentnummer
US06162937

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