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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2099708Erstellt: 25. Oktober 2026

Acetic Acid → [2-(3,4-Dimethoxy-phenyl)-1-methyl-ethyl]-ethyl amine

https://huagongshe.com/reaction/2099708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktEthylamineHCID 6341—
Edukt2-Propanone, 1-(3,4-dimethoxyphenyl)-HCID 69896—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
Produkt[2-(3,4-Dimethoxy-phenyl)-1-methyl-ethyl]-ethyl amineHCID 2206157092%

Reaktionsschritte

A solution of 10 g (51.4 mmol) of 3,4-dimethoxyphenylacetone in 50 mL of methanol was cooled to 0° C. and was treated with 50 mL of 2M solution of ethylamine in methanol. To the reaction mixture 11.5 g (0.183 mmol) of sodium cyanoborohydride was added, and the pH of the reaction mixture was adjusted to 6.5-7 by adding glacial acetic acid. The mixture was allowed to stir at room temperature for 4 days. This was concentrated under reduced pressure, and 150 mL of water was added. The pH of the resulting solution was adjusted to 1 using 6 N HCl. This was extracted with 4×150 mL of ether and the organic layers were discarded. The pH of the aqueous layer was adjusted to 14, and the solution was extracted with 6×100 mL of chloroform. The organic layers were combined, dried (Na2SO4) and concentrated to dryness to give 10.6 g (47.4 mmol, 92%) of 2A as a pale yellow oil (M+H, 224).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07569676B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-0fb2d5e7f40e4532b272da36311ba088
Quellennotizuspto-grants-2009_08