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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1637301Erstellt: 26. Oktober 2026

2,4-Dimethyl-6-tert-butylphenol → 4-(4-Methacryloyloxybutoxy)phenyl 4-allyloxybenzoate

https://huagongshe.com/reaction/1637301

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Dimethyl-6-tert-butylphenolHCID 15884—
Edukt4-(4-Bromobutoxy)phenyl 4-allyloxybenzoateHCID 19348983—
EduktPotassium methacrylateHCID 23667354—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt4-(4-Methacryloyloxybutoxy)phenyl 4-allyloxybenzoateHCID 2199961883%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

118.4 g (0.29 mol) of this ester were dissolved in 50 ml of dimethylformamide at 70° C., 0.3 g of 2-tert-butyl-4,6-dimethylphenol was added as stabilizer, 111.7 g (0.9 mol) of dry potassium methacrylate salt were added, and the mixture was diluted with 70 ml of toluene. The reaction mixture was stirred at 100° C. for 6 h, then cooled and diluted with 800 ml of methyl tert-butyl ether. The precipitate was filtered off with suction, and the washing solution and the filtrate were combined and washed three times with water. They were then concentrated, and the crude product obtained was recrystallized from isopropanol. 4-(4-Methacryloyloxybutoxy)phenyl 4-allyloxybenzoate of m.p. 62-63° C. was obtained in a yield of 83%. Between 41 and 45° C. the ester has a nematic phase which occurs only on supercooling.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06040411
Quelldatensatzuspto-grants-2000_03
ORD IDord-f2119b27a66f42e48695240ef4e4ba8d
Quellennotizuspto-grants-2000_03