Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 536221Erstellt: 24. Oktober 2026

Triethylamine → Triethylammonium bromide

https://huagongshe.com/de/reaction/536221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktCyanogen BromideHCID 10476—
Edukt2-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxyanilineHCID 58377357—
LösungsmittelDichloromethaneHCID 6344—
ProduktTriethylammonium bromideHCID 2734074296,1%
ProduktHCID 178488375HCID 178488375—

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

2-(4,5-Dihydro-1H-imidazol-2-yl)-6-methoxyaniline (Step 3, 22.0 g, 115 mmol) and Et3N (48.1 mL, 345 mmol) were dissolved in CH2Cl2 (200 mL), cooled to 10° C. in an ice bath and cyanogen bromide (24.4 g, 230 mmol) was added portionwise. A slight exotherm was noted, and the reaction was stirred overnight. The reaction was concentrated under reduced pressure, then treated with EtOAc (150 mL) and concentrated under reduced pressure again. Finally, the residue was treated with Heptane and concentrated under reduced pressure to give the title compound as a mixture with Et3N.HBr (62 g, 99%): HPLC MS RT=1.08 min, MH+=217.1; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 3.85 (3H, s), 4.09-4.16 (2H, m), 4.31-4.38 (2H, m), 7.23 (1H, t), 7.31 (1H, d), 7.57 (1H, dd).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859572B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-cbf1799c49494e7eaaac2cf948a53bb4
Quellennotizuspto-grants-2014_10