1,3-Cyclopentadiene, 5-(1-methylethylidene)- → HCID 131720872, Verbindung

HRID 399296Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 399296
[C:1]1([CH-:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[K+].[CH3:15][C:16]([CH3:22])=[C:17]1[CH:21]=[CH:20][CH:19]=[CH:18]1>C1COCC1>[CH:17]1([C:16]([CH3:22])([CH3:15])[CH:7]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH:21]=[CH:20][CH:19]=[CH:18]1

Komponenten

4

Edukt 2

HCID 1374671,3-Cyclopentadiene, 5-(1-methylethylidene)-HCID 11858962Potassium, (diphenylmethyl)-

Produkt 1

HCID 131720872HCID 131720872, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

Potassium diphenylmethanide (5.72 g, 27.8 mmols) in about 50 mL of THF was slowly added to 6,6-dimethylfulvene (2.94 g, 27.8 mmols) in about 100 mL of THF at about 25 C. The reaction mixture was stirred at about 25° C. for about 16 hours. The solvent was removed under reduced pressure to give the desired product as a sticky, oily solid.

Aufarbeitung

  1. customThe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-977dbb3c7fbe44209e362dc473b9d505
Quelldatensatz
uspto-grants-1998_10
Patentnummer
US05817849

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