Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15698Erstellt: 24. Oktober 2026

Water → {2-(2,3,4,5-Tetramethylcyclopentadienyl)phenyl}phenylmethylalcohol

https://huagongshe.com/de/reaction/15698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTolueneHCID 1140—
Edukt2-(2,3,4,5-Tetramethylcyclopentadienyl)benzaldehydeHCID 131727115—
EduktHCID 178506676HCID 178506676—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelCyclohexaneHCID 8078—
Produkt{2-(2,3,4,5-Tetramethylcyclopentadienyl)phenyl}phenylmethylalcoholHCID 13172711687%

Reaktionsschritte

To a solution of 2-(2,3,4,5-tetramethylcyclopentadienyl)benzaldehyde (2.0 g, 8.80 mmol) in tetrahydrofuran (34.0 mL) was added dropwise a 1.05 M solution of phenyllithium in cyclohexane and ether (17.7 mL) at −78° C. The temperature of the mixture was raised to room temperature and the mixture was stirred for 4 hrs. To the reaction mixture solution were added deionized water (20.0 mL) and toluene (20.0 mL) to separate an organic layer and an aqueous layer. The organic layer was dried over sodium sulfate, then distilled to remove the solvent, and purified by a silica gel column (hexane/ethyl acetate=9/1) to give {2-(2,3,4,5-tetramethylcyclopentadienyl)phenyl}phenylmethylalcohol (2.83 g, yield 87.0%) as a pale yellow oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732643B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-26e9f2d2099144b3b3ab23636d67b9e4
Quellennotizuspto-grants-2010_06