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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 371768Erstellt: 25. Oktober 2026

Triphenylphosphine → [4-(Methanesulfonylaminocarbonyl)butyl]triphenylphosphonium bromide

https://huagongshe.com/reaction/371768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt5-Bromo-N-methanesulfonylpentanamideHCID 20296141—
LösungsmittelAcetonitrileHCID 6342—
Produkt[4-(Methanesulfonylaminocarbonyl)butyl]triphenylphosphonium bromideHCID 1960884063,7%

Reaktionsschritte

A solution of 2.20 g. (8.57 mmoles) of the N-methanesulfonyl-5-bromovaleramide, prepared as above, 2.24 g. (8.57 mmoles) of triphenylphosphine, and 20 ml. of acetonitrile was heated to reflux under nitrogen overnight. The solution was then concentrated by rotary evaporation and the resultant solid was triturated with hot benzene (4X). The triturated solid was recrystallized from absolute ethanol:ether to afford the white, crystalline [4-(methanesulfonylaminocarbonyl)butyl]triphenylphosphonium bromide weighing 2.80 g. (63.7% yield) melting at 190°-191°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04087604
Quelldatensatzuspto-grants-1978_05
ORD IDord-9611f217bbcd4502bb65382299ff236c
Quellennotizuspto-grants-1978_05