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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 222501Erstellt: 23. Oktober 2026

Phenol → 3-Bromodiphenyl ether

https://huagongshe.com/de/reaction/222501

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktCesium carbonateHCID 10796—
Edukt1,2-DibromobenzeneHCID 11414—
EduktBut-3-enyl-((S)-1-phenyl-ethyl)-amineHCID 10559173—
KatalysatorHCID 178419072HCID 178419072—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt3-Bromodiphenyl etherHCID 9616553%

Reaktionsbedingungen

Temperatur195 °C

Reaktionsschritte

1-Bromo-3-phenoxy-benzene (A) A mixture of dibromobenzene (3 g, 12.75 mmol), phenol (1 g, 10.6 mmol), copper(I) oxide (152 mgs, 1 mmol), and cesium carbonate (3.46 g, 10.6 mmol) in 8 mL of NMP is heated at 195° C. for 20 minutes in a microwave. The heterogeneous mixture is filtered through a bed of Celite and the residue is washed with EtOAc (1×20 mL). The filtrate is diluted with 1N NaOH (200 mL) and extracted with EtOAc (3×100 mL). The organics were combined, dried over Na2SO4, filtered and concentrated under reduced pressures to give crude product as a yellow oil which is purified by column chromatography (100% hexanes) to give 1-bromo-3-phenoxy-benzene as a colorless oil (1.4 g, 53%). LCMS m/z 250 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207183B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f99cacf8174a426aaa164c36ef6fbb4d
Quellennotizuspto-grants-2012_06