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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2229988Erstellt: 25. Oktober 2026

Ethylparaben → 4-(4-Hydroxybutoxy)benzoic acid

https://huagongshe.com/reaction/2229988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylparabenHCID 8434—
EduktPotassium CarbonateHCID 11430—
Edukt1-Butanol, 4-chloro-, 1-acetateHCID 23399—
KatalysatorPotassium IodideHCID 4875—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-Hydroxybutoxy)benzoic acidHCID 1521859689,5%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

276.6 g of 4-chlorobutyl acetate (1.8 mol) were added to a solution of 249 g of ethyl 4-hydroxybenzoate (1.5 mol), 3 g of potassium iodide (0.018 mol) and 248 g of potassium carbonate (1.8 mol) in 2 l of DMF, and the mixture was stirred at 90° C. for 11 hours. The reaction mixture was poured into 5 l of ice-water, and the precipitate was filtered off with suction and washed with 4 l of ice-water. The crude product was dissolved in 3 l of ethanol, potassium hydroxide (400 g) was added, and the mixture was refluxed for 3 hours. The reaction mixture was poured into 6 l of ice-water and acidified using concentrated hydrochloric acid, and the precipitate was filtered off. The precipitate was washed with water until neutral and then dried, giving 282.1 g of 4-(4′-hydroxybutoxy)benzoic acid (yield 89%). b) A solution of 282 g of 4-(4′-hydroxybutoxy)benzoic acid (1.34 mol), 230 ml of freshly distilled acrylic acid (3.35 mol), 0.3 g of 2,6-di-tert-butyl-4-(dimethylaminomethylene)phenol (Ethanox® 703) and 23.7 g of p-toluenesulfonic acid in 1.1 liter of 1,1,1-trichloroethane was refluxed for 10 hours on a water separator. The reaction mixture was cooled to 60° C.-70° C. and stirred into 2.5 l of petroleum ether, and the precipitate was filtered off. After washing with petroleum ether, the precipitate was dried for 24 hours at room temperature under reduced pressure, giving 223.7 g of 4-(4′-acryloxybutoxy)benzoic acid (yield 60%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06423246B1
Quelldatensatzuspto-grants-2002_07
ORD IDord-f48699e7a4974519b82c87b8cfb1f715
Quellennotizuspto-grants-2002_07