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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 588548Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/588548

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
PatentnummerUS09227940B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-f260772959b8468aaa409be04952dbaf
Quellennotizuspto-grants-2016_01