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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346930Erstellt: 25. Oktober 2026

Methyl iodide → N-tert-butyl-1-methylcyclopropane-1-sulfonamide

https://huagongshe.com/reaction/346930

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktN-tert-butyl-3-chloropropane-1-sulfonamideHCID 11701296—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-tert-butyl-1-methylcyclopropane-1-sulfonamideHCID 2188979281%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of N-tert-butyl-(3-chloro)propylsulfonamide (4.3 g, 20 mmol) was dissolved in dry THF (100 mL) and cooled to −78° C. To this solution was added n-BuLi (17.6 mL, 44 mmol, 2.5 M in hexane) slowly. The dry ice bath was removed and the reaction mixture was allowed to warm to rt over a period of 1.5 h. This mixture was then cooled to −78° C., and a solution of n-BuLi (20 mmol, 8 mL, 2.5 M in hexane) was added. The reaction mixture was warmed to rt, recooled to −78° C. over a period of 2 h and a neat solution of methyl iodide (5.68 g, 40 mmol) added. The reaction mixture was allowed to warm to rt overnight, quenched with saturated NH4Cl (100 mL) at rt. It was extracted with EtOAc (100 mL). The organic phase was washed with brine (100 mL), dried (MgSO4), and concentrated in vacuo to give a yellow oil which was crystallized from hexane to afford the product as a slightly yellow solid (3.1 g, 81%): 1H NMR (CDCl3) δ 0.79 (m, 2H), 1.36 (s, 9H), 1.52 (m, 2H), 1.62 (s, 3H), 4.10 (bs, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173004B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-5a6d61a506144cb6ae560b60dce21783
Quellennotizuspto-grants-2007_02