Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17098Erstellt: 23. Oktober 2026

Formamide → 1-(3-Bromophenyl)ethanamine

https://huagongshe.com/de/reaction/17098

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormamideHCID 713—
Edukt3'-BromoacetophenoneHCID 16502—
LösungsmittelFormic AcidHCID 284—
Produkt1-(3-Bromophenyl)ethanamineHCID 16785764—

Reaktionsbedingungen

Temperatur220 °C

Reaktionsschritte

A mixture of commercially available 3-bromoacetophenone (30 g, 0.1508 mol), formic acid (47 mL) and formamide (70 mL) was heated to 220° C. for 5 h. The brown liquid obtained was cooled to RT, quenched with water and extracted with ethyl acetate. The organic layer was washed with water, brine and concentrated. The resulting brown liquid was dissolved in ethanol (375 mL) and conc. HCl (75 mL) and the mixture was refluxed over night. Ethanol was removed completely and the aqueous layer was washed with ether and ethyl acetate to remove all non-basic impurities. The aqueous layer was basified with a 10% aqueous sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, and concentrated to provide 26 g (86.65%) of A56.1. This compound was taken to the next step with out further purification. 1H NMR (CDCl3, 300 MHz) δ 1.38 (d, 3H), 4.1 (q, 1H), 7.2 (m, 1H), 7.27 (m, 1H), 7.37 (m, 1H), 7.51 (s, 1H). LS-MS (M−H)+=200.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737279B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e802393c4399432983187cfefc702fd7
Quellennotizuspto-grants-2010_06