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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 366892Erstellt: 25. Oktober 2026

Sulfuric Acid → 1-Benzyl-4-phenyl-3-pyrrolidinol

https://huagongshe.com/reaction/366892

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTetrahydrofuranHCID 8028—
Edukt1-Benzyl-2,5-dihydropyrroleHCID 561506—
EduktHCID 178506676HCID 178506676—
LösungsmittelWaterHCID 962—
LösungsmittelCyclohexane diethyletherHCID 21895417—
Produkt1-Benzyl-4-phenyl-3-pyrrolidinolHCID 1204405376,3%

Reaktionsschritte

To a solution of 15.9 g (0.1 mol) of 1-benzyl-3-pyrroline, 12.0 g (0.12 mol) of 98% sulfuric acid, and 60.0 g of THF in a quartz round flask reactor, 45.6 g (0.20 mol) of (NH4)2S2O8 (ammonium peroxydisulfate produced by Mitsubishi Gas Chemical Industry Co., Ltd.) was added with stirring and allowed to react for 5 days at room temperature with irradiation by 500 W Xe lamps (UXL-500D xenon lamp produced by Ushio). 300 mL (0.30 mol) of 1 mol/L phenyllithium (PhLi) in cyclohexane-diethyl ether solution (produced by Kanto Chemical Co., Inc.) was continuously added to the reaction mixture and stirred for 5 hours at about 5° C. using an ice-bath. After completion, water was added to destroy excess PhLi at about 5° C. using an ice-bath. Acetone and diethyl ether were evaporated under reduced pressure, and extracted with toluene and water. After the solvent was evaporated under reduced pressure, 19.3 g of 1-benzyl-4-phenyl-3-pyrrolidinol (yield 76.3%) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06130338
Quelldatensatzuspto-grants-2000_10
ORD IDord-8ab590d5a6c34c8691c591d23268d7e4
Quellennotizuspto-grants-2000_10