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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 839813Erstellt: 24. Oktober 2026

Hydrochloric Acid → N-methyl-5-(4-nitrophenyl)-N-(a-methylphenethyl)furfurylamine hydrochloride

https://huagongshe.com/de/reaction/839813

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethanolHCID 887—
EduktMethamphetamineHCID 10836—
Edukt2-(Chloromethyl)-5-(4-nitrophenyl)furanHCID 15212084—
LösungsmittelBenzeneHCID 241—
ProduktN-methyl-5-(4-nitrophenyl)-N-(a-methylphenethyl)furfurylamine hydrochlorideHCID 2032216667,2%

Reaktionsschritte

A solution of 11.9 g (0.05 mole) of 5-(4-nitrophenyl)furfuryl chloride and 14.9 g (0.10 mole) of d-N,a-dimethylphenethylamine in 60 ml of benzene was heated under reflux for 7 hrs. After standing overnight, the solid N,a-dimethylphenethylamine hydrochloride (9 g, 97%) was collected by filtration and washed with benzene. The benzene filtrate was washed with 10% Na2CO3 and water and dried over MgSO4. The solvent was removed on a rotary evaporator, and the residual oil was dissolved in 100 ml of anhydrous ether and 35 ml of nhydrous MeOH. The solution was treated with 20 ml of ethereal HCl and diluted with ether to give an oil. The solvent was removed on a rotary evaporator, and the residual oil was dissolved in ethyl acetate with heating. Cooling gave an oil which was dissolved by the addition of MeOH and 10 ml of etheral HCl. After cooling and dilution with ether, the yellow solid which was deposited was collected by filtration to give 13 g (67%) of N-methyl-5-(4-nitrophenyl)-N-(a-methylphenethyl)furfurylamine hydrochloride; m.p. 168°-175°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04097500
Quelldatensatzuspto-grants-1978_06
ORD IDord-dca4f4ab0b6848b2ac5d24f2832de2d1
Quellennotizuspto-grants-1978_06