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HRID 456374Erstellt: 24. Oktober 2026

Chlorotrimethylsilane → 2-(4-(N-salicyloyl)aminophenyl)propionic acid

https://huagongshe.com/de/reaction/456374

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktTriethylamineHCID 8471—
Edukt4-Aminohydratropic acidHCID 43026—
Edukt2-Acetoxybenzoyl chlorideHCID 79668—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(4-(N-salicyloyl)aminophenyl)propionic acidHCID 981730352,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A slurry of 58.6 g (0.355 mol) of 2-(4-aminophenyl)propionic acid and 500 ml of methylene chloride is treated with 90.11 ml (77.13 g. 0–710 mol) of trimethylsilyl chloride and is heated to reflux for 120 min. The reaction mixture is cooled to 0° C. and treated with 184.44 ml (107.77 g, 1.065 mol) of triethylamine. After stirring for 5 minutes, this mixture is treated with a solution of 70.45 g (0.355 mol) of O-acetylsalicyloyl chloride and 150 ml of methylene chloride. The reaction mixture is warmed to 25° C. and stirred for 64 hr. The volatiles are removed in vacuo. The residue is stirred in 2N aqueous sodium hydroxide for one hour and acidified with 2 M aqueous sulfuric acid. The solid is recrystallized twice from ethanol/water to give a tan solid. Isolation by filtration results in an expected yield of 53.05 g (52% yield) of 2-(4-(N-salicyloyl)aminophenyl)propionic acid. Properties. Solubility: 200 mg/m: 200 mg+350 μL 2N NaOH+650 μL H2O-pH-7.67. Analysis: C, 67.36; H, 5.3; N, 4.91.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07186691B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-90030ab3e14f4ae295ed31050ef8ba7f
Quellennotizuspto-grants-2007_03