Water → Acetylfluorene

HRID 484741

Reaktionsgleichung

Reaktionsgleichung von HRID 484741
[C:1]1([C:14](O)=[O:15])[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH3:17][Li].O>O1CCCC1>[C:14]([C:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1)(=[O:15])[CH3:17]

Komponenten

5

Edukt 3

HCID 962WaterHCID 80468Fluorene-1-carboxylic acidHCID 178418348HCID 178418348, Verbindung

Produkt 1

HCID 13520055Acetylfluorene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 108 g. of 1-fluorenecarboxylic acid in 2 liters of dry tetrahydrofuran cooled to -78° C. by means of an external dry ice/acetone bath were added 2 moles of methyl lithium (6 molar solution in diethyl ether). The reaction was stirred at room temperature for 3 hours and then poured into 3 liters of water. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated in vacuo. The residue was chromatographed over silica gel. The appropriate fractions were combined and evaporated to dryness. Recrystallization of the residue from ethyl acetate/hexane gave 1-acetylfluorene, m.p. 84°-87° C.

Aufarbeitung

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with ethyl acetate
  3. dry with materialThe combined organic layers were dried over sodium sulfate
  4. customevaporated in vacuo
  5. customThe residue was chromatographed over silica gel
  6. customevaporated to dryness
  7. customRecrystallization of the residue from ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-736bd308c97f4f2e9ec527ec9f736045
Quelldatensatz
uspto-grants-1985_08
Patentnummer
US04533670

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