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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76918Erstellt: 24. Oktober 2026

Benzyl Bromide → HCID 86634679, Verbindung

https://huagongshe.com/de/reaction/76918

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktHexaneHCID 8058—
Edukt3-MethoxypropyneHCID 69393—
EduktLithium BromideHCID 82050—
Edukt4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
EduktButyllithiumHCID 178418339—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 86634679HCID 86634679—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

Methyl propargyl ether (0.36 g, 5.2 mmol) dissolved in abs. THF (5 mL) was added in drops to a 2.5 M solution of butyl lithium in hexane (2.1 mL, 5.2 mmol) at −30° C. in argon. A solution of 4-dimethylamino-4-phenylcyclohexanone (1.08 g, 5.0 mmol) in abs. THF (5 mL) and lithium bromide (0.22 g, 2.5 mmol) dissolved in abs. THF (2.0 mL) was then added at −30° C. The reaction mixture was heated to −5° C., mixed in drops with a solution of benzyl bromide (1.28 g, 7.5 mmol) in abs. DMSO (10 mL) and stirred 2 h at 50° C. For work up of the reaction mixture water (10 mL) was added with ice bath cooling and extracted with cyclohexane (4×20 mL). The organic phase was washed with 20% ammonium chloride solution, dried over Na2SO4 and concentrated to low volume in a vacuum. The remaining residue was purified by flash chromatography with CHCl3/MeOH (40:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835689B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-a9aa16dfd7fd4cdfac553552dfcd70be
Quellennotizuspto-grants-2014_09