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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 504273Erstellt: 25. Oktober 2026

1-Benzyl-3-pyrrolidinone → HCID 66661626, Verbindung

https://huagongshe.com/reaction/504273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-3-pyrrolidinoneHCID 69890—
EduktN-(1,1-Dimethylethyl)benzenesulfonamideHCID 314059—
EduktHCID 178418306HCID 178418306—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelPentaneHCID 8003—
ProduktHCID 66661626HCID 6666162639,5%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of N-(tert-butyl)benzenesulfonamide (536 mg, 0.00251 mol) in ether (10 mL, 0.1 mol) was added 1.7 M of tert-butyllithium in pentane (4.4 mL) under nitrogen at −78° C. The mixture was stirred at −78 Celsius for 15 min, then at 0 Celsius for 1 hour, and then cooled down to −78 Celsius again. A solution of 1-benzylpyrrolidin-3-one (400.0 mg, 0.002283 mol) in ether (3 mL) was added to the above solution. The reaction solution was stirred at ±78 Celsius for 2 hours, then quenched with saturated NH4Cl aqueous solution, and then extracted with EtOAc. The organic phase was washed with brine, then dried over MgSO4. The residue was purified by flash chromatography on silica gel column with 30% AcOEt in hexanes to give the desired compound (350 mg, 39% yield). MS (ESI): 389.1 (M+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07776874B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-38a87060dc734d9e96bdeea77f1db806
Quellennotizuspto-grants-2010_08