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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484681Erstellt: 24. Oktober 2026

2,6-Dimethoxybenzoyl chloride → (3S-trans)-3-[(2,6-dimethoxybenzoyl)amino]-4-methyl-1-[(phenylmethyl)oxy]-2-azetidinone

https://huagongshe.com/de/reaction/484681

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-Dimethoxybenzoyl chlorideHCID 74810—
EduktToluenesulfonateHCID 3424274—
Edukt(3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinoneHCID 13036842—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3S-trans)-3-[(2,6-dimethoxybenzoyl)amino]-4-methyl-1-[(phenylmethyl)oxy]-2-azetidinoneHCID 13036849—

Reaktionsschritte

To a cold (-10° C.) solution of (3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinone, toluenesulfonate (0.95 g; see example 2D) in methylene chloride (50 ml) is added 2,6-dimethoxybenzoyl chloride (0.60 g) and 4-dimethylaminopyridine (0.61 g). The reaction is stirred under nitrogen and allowed to rise to 26° C. over five hours. The reaction mixture is concentrated to an oil and partitioned between ethyl acetate and aqueous hydrogen sulfate solution. The organic layer is washed with aqueous sodium bicarbonate, and brine, dried over sodium sulfate and concentrated to a foam (0.848 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04533660
Quelldatensatzuspto-grants-1985_08
ORD IDord-b3c4aefaa8124d5eaa3567e0899a03f9
Quellennotizuspto-grants-1985_08