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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1836773Erstellt: 26. Oktober 2026

2-Phenylisobutyric acid → 2-[4-(4-Chloro-butyryl)-phenyl]-2-methyl-propionic acid pyrrolidineamide

https://huagongshe.com/reaction/1836773

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Phenylisobutyric acidHCID 13222—
Edukt4-Chlorobutyryl chlorideHCID 78370—
Edukt1-PyrrolidinecarboxamideHCID 138335—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt2-[4-(4-Chloro-butyryl)-phenyl]-2-methyl-propionic acid pyrrolidineamideHCID 6989465078%

Reaktionsschritte

Add AlCl3 (8.31 g, 62.3 mmol) to carbon tetrachloride (65 mL) under a nitrogen atmosphere at room temperature. Add 4-chlorobutyryl chloride (03.5 mL, 31.2 mmol), stir for 15 minutes and add, by dropwise addition over 15 minutes, a solution of 2-methyl-2-phenyl-propionic acid, pyrrolidineamide (5.64 g, 26.0 mmol) in carbon tetrachloride (60 mL). Stir at room temperature for 17 hours, pour into ice water (100 mL) and separate the layers. Wash the aqueous layer with methylene chloride (2×70 mL), 5% aqueous sodium hydrogen carbonate, combine the organic layers and dry (Na2SO4). Filter, evaporate the filtrate in vacuo and purify by silica gel chromatography (5:2 hexane/ethyl acetate) to give the title compound (6.559, 78%) as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06777555B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-c661aa5fc1944b339fb70ceea8a1b969
Quellennotizuspto-grants-2004_08