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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247721Erstellt: 25. Oktober 2026

Phenol → Benzenemethanol, 3-phenoxy-, 1-acetate

https://huagongshe.com/reaction/247721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktPotassium HydroxideHCID 14797—
EduktBenzenemethanol, 3-bromo-, 1-acetateHCID 12858554—
LösungsmittelO-XyleneHCID 7237—
ProduktBenzenemethanol, 3-phenoxy-, 1-acetateHCID 17090477%

Reaktionsschritte

10.35 g. (0.11 mole) of phenol, 6.15 g. (0.11 mole) of potassium hydroxide and 35 cm3. of xylene are weighed together. The water is azeotropically distilled with stirring and boiling. 5 cm3. of pyridine and 0.5 g. of copper(I) chloride are added then 22.91 g. (0.1 mole) of 3-bromobenzyl acetate are dropped into the reaction mixture during 15 minutes with stirring and boiling. The reaction mixture is boiled with stirring for an additional three hours. After cooling the reaction mixture is filtered off and the filtrate washed with a mixture of 25 cm3. of 15% sodium chloride solution and 2 cm3. of 40% sodium hydroxide solution. The organic phase is evaporated in vacuo. The residue is distilled in vacuo and so 18.65 g. of 3-phenoxybenzyl acetate are obtained. Boiling point 142°-145° C./53.2 Pa, nD20 : 1.5621, yield 77%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04709081
Quelldatensatzuspto-grants-1987_11
ORD IDord-9324d319bedd4b14a18344d4054d26d2
Quellennotizuspto-grants-1987_11