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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40499Erstellt: 25. Oktober 2026

N-((1S)-1-(4-Bromophenyl)ethyl)acetamide → (S)-N-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-azetidin-1-yl]-phenyl}-ethyl)-acetamide

https://huagongshe.com/reaction/40499

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-((1S)-1-(4-Bromophenyl)ethyl)acetamideHCID 793484—
Edukt2-(Di-tert-butylphosphino)biphenylHCID 2734215—
EduktSodium t-butoxideHCID 23676156—
Edukt3-((tert-Butyldimethylsilanyl)oxy)azetidineHCID 57438656—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(S)-N-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-azetidin-1-yl]-phenyl}-ethyl)-acetamideHCID 86689004—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 3.0 g (12.4 mmol) (S)—N-[1-(4-bromo-phenyl)-ethyl]-acetamide (I.1), 2.3 g (12.4 mmol) 3-(tert-butyl-dimethyl-silanyloxy)-azetidine (US2008/214520A1), 4.9 g (97%, 49.6 mmol) NaOtBu, 1.48 g (4.96 mmol) 2-(di-tert-butylphosphino)biphenyl and 1.1 g (1.24 mmol) tris-(dibenzylideneacetone)-dipalladium(0) in 30 mL 1,4-dioxane is stirred for 45 min under microwave irradiation at 80° C. After cooling water and MeOH are added, the mixture is filtered, concentrated in vacuo and directly purified by HPLC (column: XbridgeC18; eluent A: water+0.3% NH4OH, eluent B: MeOH) to yield the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530461B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-dcd68dc0bcee42018476560e3ed1afa3
Quellennotizuspto-grants-2013_09