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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1056923Erstellt: 26. Oktober 2026

Benzaldehyde → Benzylidene-(3-bromo-1-propylamine)

https://huagongshe.com/reaction/1056923

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktTriethylamineHCID 8471—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Edukt3-BromopropylamineHCID 78702—
LösungsmittelChloroformHCID 6212—
ProduktBenzylidene-(3-bromo-1-propylamine)HCID 11053338100%

Reaktionsschritte

The hydrobromide salt of 3-bromopropylamine (5.364 g, 24.50 mmol) was treated with triethylamine (4 mL) in CHCl3 (100 mL) and allowed to stir at room temperature for 5 min. Benzaldehyde (2.000 g, 18.85 mmol) and magnesium sulfate (6.000 g) were added and the reaction mixture was allowed to stir at room temperature for 16 h. The reaction mixture was filtered and the filter pad was washed with CHCl3 (50 mL). The filtrate was washed with water (3×50 mL), sat NaCl (50 mL), dried over sodium sulfate, and concentrated to provide a yellow oil (4.262 g, 100%). IR (film) 1645, 754, and 693 cm−1; 1H NMR (CDCl3) δ 8.34 (s, 1H), 7.76 (m, 2H), 7.44 (m, 3H), 3.78 (dt, J=6.3 Hz and 1.3 Hz, 2H), 3.52 (t, J=6.5 Hz, 2H), 2.31 (pent, J=6.4 Hz, 2H); ESIMS m/z (rel intensity) 226/228 (MH+, 100/91). Anal. (C10H12BrN) C, H, N.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09399660B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-16deeed8a8bf44db90a43b8645e27a76
Quellennotizuspto-grants-2016_07