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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 229561Erstellt: 25. Oktober 2026

Bupropion → Bupropion toluene

https://huagongshe.com/reaction/229561

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBupropionHCID 444—
EduktTert-ButylamineHCID 6385—
EduktBromineHCID 24408—
Edukt3-ChloropropiophenoneHCID 70295—
LösungsmittelDichloromethaneHCID 6344—
ProduktBupropion tolueneHCID 66960545—

Reaktionsschritte

3-Chloro-propiophenone starting material was brominated in methylene chloride by dropping bromine under controlled conditions. On reaction completion the mother liquor was worked up and then the second reaction was executed by transferring the bromoderivative solution onto the tert-butylamine. The second substitution reaction (the tert-butylamine amino-group substitutes the bromine atom) forms the final bupropion molecule. After work up of the mother liquor, a bupropion toluene solution was obtained. The solvent was evaporated and bupropion was dissolved in isopropanol. From the isopropanol solution, the hydrobromide was precipitated with hydrogen bromide gas. On precipitation completion, the product was centrifuged, washed with isopropanol and dried under vacuum. On dryer discharge approval it was discharged in Kraft drums within double polyethylene bags.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07563823B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-605f58bacf674a288929e4698d912980
Quellennotizuspto-grants-2009_07