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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132104Erstellt: 26. Oktober 2026

Cyclohexanone → 1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanol

https://huagongshe.com/reaction/132104

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexanoneHCID 7967—
EduktPentaneHCID 8003—
Edukt1-Bromo-3-tert-butylbenzeneHCID 343798—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanolHCID 5973374381%

Reaktionsschritte

A solution of 1.7 M tert-butyllithium in pentane (32.0 mL, 54.4 mmol) was added to a solution of 1-bromo-3-tert-butyl-benzene (5.54 g, 26.0 mmol) in tetrahydrofuran (60 mL) at −78° C. After stirring for 1 h, cyclohexanone (2.00 g, 18.2 mmol) in tetrahydrofuran (15 mL) was added. After stirring for 18 h, during which time the solution warmed to ambient temperature, the solution was diluted with saturated aqueous ammonium chloride and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was flash chromatographed with 49:1, 24:1, 23:2 hexanes:ethyl acetate as the eluant to yield 3.61 g (81% yield) of 1-(3-tert-butyl-phenyl)-4-methylene-cyclohexanol as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07385085B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-f0668dfcdcd04782a255a587cf61429e
Quellennotizuspto-grants-2008_06