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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26084Erstellt: 24. Oktober 2026

Dimethylformamide → 3-(Benzyloxy)-4-bromophenol

https://huagongshe.com/de/reaction/26084

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktBenzyl BromideHCID 7498—
Edukt4-BromoresorcinolHCID 81105—
EduktPotassium hydrideHCID 82127—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-(Benzyloxy)-4-bromophenolHCID 15670654—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a 0° C. slurry of 1.7 g. (42.5 mmoles) of potassium hydride in 35 ml. of N,N-dimethylformamide is slowly added a solution of 7.22 g. (38.2 mmoles) of 4-bromoresorcinol. The resultant mixture is stirred for 30 minutes and then 4.54 ml. (38.2 mmoles) of benzyl bromide is slowly added. The reaction mixture is stirred 3 hours longer at 0° C. and then added to 200 ml. of cold water and 200 ml. of ether. The ether extract is washed twice with 200 ml. portions of water, dried over magnesium sulfate and evaporated to an oil. The crude oil is purified via column chromatography on 400 g. of silica gel eluted with 25% ether-pentane to yield (in order of elution) 2.2 g. (16%) of 2,4-dibenzyloxybromobenzene, 0.21 g. (2%) of 5-benzyloxy-2-bromophenol and 3.52 g. (33%) of 3-benzyloxy-4-bromophenol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147872
Quelldatensatzuspto-grants-1979_04
ORD IDord-cbaf3fd342894c14a78febb86ca2b7a8
Quellennotizuspto-grants-1979_04