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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275419Erstellt: 26. Oktober 2026

Hydrochloric Acid → (+-)-p-Methoxyamphetamine

https://huagongshe.com/reaction/275419

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4'-MethoxyacetophenoneHCID 7476—
EduktAmmonium AcetateHCID 517165—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
Produkt(+-)-p-MethoxyamphetamineHCID 31721—

Reaktionsschritte

A solution of 32 g (0.21 mol) of 4'-methoxyacetophenone and 165 g (2.1 mol) of ammonium acetate in 450 ml of methanol is combined with 13.5 g (0.21 mol) of sodium cyanoborohydride, which is added in batches thereto at ambient temperature, with stirring. After a further 20 hours, ice is added and the mixture is acidified with hydrochloric acid (conc. HCl H2O=1/1) until the pH is 2. The acidic solution is extracted with dichloromethane. The aqueous phase is then mixed with conc. ammonia, with cooling, until a clearly alkaline reaction occurs and then extracted exhaustively with dichloromethane. The combined dichloromethane extracts are dried over sodium sulphate and evaporated to dryness in vacuo. The crude 2-(4-methoxyphenyl)-1-methylethylamine thus obtained is purified by column chromatography over silica gel (eluant: dichloro-methane/methanol=20/1) to remove any by-products. A colorless oil is obtained which can be used for reaction without any further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05393774
Quelldatensatzuspto-grants-1995_02
ORD IDord-ca523392809241f08caa36aabdb2c1c5
Quellennotizuspto-grants-1995_02