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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49212Erstellt: 23. Oktober 2026

Chloride → 4-methyl-2H-isoquinolin-1-one

https://huagongshe.com/de/reaction/49212

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorideHCID 312—
EduktTriethylamineHCID 8471—
EduktN-Allyl-2-iodobenzamideHCID 2190306—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-methyl-2H-isoquinolin-1-oneHCID 12695299—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Under an N2 atmosphere, 985 ml (7.07 mol) of triethylamine, 892 g (3.21 mol) of tetra-nbutylammonium chloride and 12.77 g (57 mmol) of Pd(OAc)2 are added to 815 g (2.8 mol) of 2-iodo-benzoic acid allylamide in 4.5 l of DMF, and heated to 100° C. After 4 h, cooling is effected to RT, and the mixture is partially concentrated by evaporation on a RE. The residue is partitioned between 5 l of water and 5 l of EtOAc, the water phase is separated and extracted twice with EtOAc. The organic phases are washed with water, 0.1 N HCl, water and brine, dried (Na2SO4) and concentrated by evaporation. Column chromatography (SiO2, EtOAc/toluene 1:1) and crystallisation from toluene yields 4-methyl-2H-isoquinolin-1-one; m.p. 175-176° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706731B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-2ee2676d0ac448f6b6ce90c56cb992e9
Quellennotizuspto-grants-2004_03