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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339156Erstellt: 24. Oktober 2026

N-tert-butyl-3-chloropropane-1-sulfonamide → N-tert-Butylcyclopropanesulfonamide

https://huagongshe.com/de/reaction/339156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-tert-butyl-3-chloropropane-1-sulfonamideHCID 11701296—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-tert-ButylcyclopropanesulfonamideHCID 2249930156,4%

Reaktionsschritte

To a solution of N-tert-butyl-(3-chloro)propylsulfonamide (2.14 g, 10.0 mmol) in THF (100 mL) was added n-BuLi (2.5 M in hexane, 8.0 mL, 20.0 mmol) at −78° C. The reaction mixture was allowed to warm up to room temperature over period of 1 h. The volatiles were removed in vacuo. The residue was partitioned between EtOAC and water (200 mL, 200 mL). The separated organic phase was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was recrystallized from hexane to yield the desired product as a white solid (1.0 g, 56%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889871B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-5f0473953fab46668f705a9dd975081f
Quellennotizuspto-grants-2014_11