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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602846Erstellt: 24. Oktober 2026

Hydrochloric Acid → 1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadiene

https://huagongshe.com/de/reaction/602846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-MethylcyclopentanoneHCID 14265—
EduktBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadieneHCID 8662956946%

Reaktionsschritte

1-Bromo-3,5-dimethylbenzene (13.6 g, 73.6 mmol) was dissolved in a mixed solution of hexane (150 mL) and diethyl ether (20 mL) and added dropwise at 0° C. with a solution (46.6 mL, 1.58M) of n-butyllithium in hexane. The solution was immediately warmed to room temperature, stirred night and day and added dropwise at −78° C. to a solution of 3-methyl-2-cyclopentanone (7.3 mL, 74 mmol) in diethyl ether (100 mL). The resultant solution was warmed to room temperature immediately after dropwise addition and stirred for 2 hours. After termination of the reaction, the reaction solution was added with dilute hydrochloric acid, stirred at room temperature for 30 minutes and then subjected to layer separation. The organic layer was dried with magnesium sulfate and then had the solvent distilled off under reduced pressure. The crude product was distilled under reduced pressure (125 to 127° C./0.5 mmHg) to obtain 1-methyl-3-(3,5-dimethyl-phenyl)-cyclopentadiene (6.2 g, yield: 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07906599B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-d148eed8c1fb41e79daedb2f1b5153da
Quellennotizuspto-grants-2011_03