Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40530Erstellt: 26. Oktober 2026

2-(Di-tert-butylphosphino)biphenyl → N-(1-{4-[3-(4-Cyclopropylmethoxy-phenoxy)-azetidin-1-yl]-phenyl}-1-methyl-ethyl)-acetamide

https://huagongshe.com/reaction/40530

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Di-tert-butylphosphino)biphenylHCID 2734215—
EduktSodium t-butoxideHCID 23676156—
EduktN-(2-(4-Bromophenyl)propan-2-YL)acetamideHCID 39616691—
Edukt3-(4-Cyclopropylmethoxy-phenoxy)-azetidineHCID 86689009—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(1-{4-[3-(4-Cyclopropylmethoxy-phenoxy)-azetidin-1-yl]-phenyl}-1-methyl-ethyl)-acetamideHCID 86689031—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To 35 mg (0.16 mmol) 3-(4-cyclopropylmethoxy-phenoxy)-azetidine (IX.1) in THF (2.0 mL) are added under an argon atmosphere 41 mg (0.16 mmol) N-[1-(4-bromo-phenyl)-1-methyl-ethyl]-acetamide, 63 mg (0.64 mmol) NaOtBu, 19 mg (0.064 mmol) 2-(di-tert-butylphosphino)biphenyl and 15 mg (0.016 mmol) tris-(dibenzylidene-acetone)-dipalladium(0). The mixture is stirred for 12 h at 45° C. The mixture is filtered and concentrated in vacuo. The residue is purified by HPLC (Zorbax, acetronitrile/H2O (+0.15% HCOOH)) to yield the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530461B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c0ff54126222457692099719ec6d4305
Quellennotizuspto-grants-2013_09