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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50012Erstellt: 24. Oktober 2026

Phenol → 1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene

https://huagongshe.com/de/reaction/50012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloro-5-nitrophenolHCID 69264—
Edukt2-Butene, 1-bromo-3-methyl-HCID 70092—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzeneHCID 12985690—

Reaktionsschritte

A reaction mixture of 2-chloro-5-nitrophenol (50.6 g), anhydrous potassium carbonate (44.5 g), tetrabutylammonium bromide (4.7 g) and 4-bromo-2-methyl-2-butene (53.3 g, 90%) in methyl ethyl ketone (263 mL) was stirred at ambient temperature overnight. TLC of the reaction mixture showed traces of phenol remaining. Additional prenyl bromide (1 mL) was then added to the reaction mixture and stirred for 2 hours. The solvent was then removed from the reaction mixture. The residue of the reaction mixture was then treated with water and extracted into diethyl ether. The extract was washed with 2N sodium hydroxide and water, dried (MgSO4), filtered, and evaporated, to leave a brown solid which was recrystallised from ethyl acetate/isopropyl alcohol to give 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene, 49.5 g, a beige solid, a single spot on TLC (ethyl acetate:hexane, 20:80).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710077B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-838b54af43ff4a799efbc77e83ff702c
Quellennotizuspto-grants-2004_03