Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357704Erstellt: 25. Oktober 2026

Pyridine → 5-(Bromomethyl)-1,2,3-trimethoxybenzene

https://huagongshe.com/reaction/357704

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktPhosphorus tribromideHCID 24614—
Edukt3,4,5-Trimethoxybenzyl alcoholHCID 77449—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(Bromomethyl)-1,2,3-trimethoxybenzeneHCID 10355271202,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 3,4,5-trimethoxybenzyl alcohol (20.2 g, 0.108 mol) in 300 ml of dry tetrahydrofuran was added 4.12 ml (0.052 mol) of pyridine, and cooled to 0° C. A solution of phosphorous tribromide (4.8 ml, 0.051 mol) in 20 ml of dry tetrahydrofuran was added dropwise to the above solution at 0 ° C. The mixture was stirred for 1 hr. Tetrahydrofuran was concentrated. The residue was then diluted with 200 ml of 10% hydrochloric acid, and then extracted with 200 ml of ethyl acetate. The extract was dried over magnesium sulfate, filtered, concentrated, and dried in vacuum overnight. 3,4,5-Trimethoxybenzyl bromide (27 g, 100% yield) was obtained as a white solid, which can be used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840991
Quelldatensatzuspto-grants-1998_11
ORD IDord-d81fec49ae5444638cd057f3f55b7c37
Quellennotizuspto-grants-1998_11