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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 439762Erstellt: 24. Oktober 2026

3-Bromophenol → Pentyl ether

https://huagongshe.com/de/reaction/439762

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromophenolHCID 11563—
EduktPentyl etherHCID 12743—
EduktBenzyl 5-Bromoamyl EtherHCID 14221121—
Edukt3-(Benzyloxypentyl)-phenolHCID 53906938—
EduktHCID 178418306HCID 178418306—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPentyl etherHCID 12743—
Produkt3-(5-Hydroxypentyl)-phenolHCID 22407972—

Reaktionsschritte

At a temperature of -78° C., 19.4 ml of t-butyl lithium (1.7M) is added to 4.0 gm of the above 3-bromo-phenol, n-pentyl ether in 50 mls tetrahydrofuran; and to this is added 3.3 ml of a freshly prepared solution of Li2CuCl3 (0.10M/THF). The mixture is stirred for 10 minutes, and then 4.35 grams of the 1-bromo-5-benzyloxy pentane are added. The reaction is allowed to warm slowly to ambient temperature over 12 hours and is then stirred an additional 24 hours before being quenched with silica gel. After removing the solvent, the mixture is chromatographed over silica gel (1:1 hexane:ether) to yield a crude mixture containing 3-(benzyloxypentyl)-phenol, n-pentyl ether. A solution of 6.0 gm of this crude mixture in ethanol is hydrogenated over 5% Pd on carbon for 5 hours. After filtering through celite and concentrating, pure 3-(5-hydroxypentyl)-phenol, n-pentyl ether is obtained as a clear oil by HPLC chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05516767
Quelldatensatzuspto-grants-1996_05
ORD IDord-89310f4a37c245118727c13c1cf2e375
Quellennotizuspto-grants-1996_05