Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1725826Erstellt: 26. Oktober 2026

Dimethylamine → 1-(7-Fluoro-1H-indol-3-yl)-N,N-dimethylmethanamine

https://huagongshe.com/reaction/1725826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktFormaldehydeHCID 712—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
Edukt7-Fluoro-1H-indoleHCID 2774504—
LösungsmittelAcetic AcidHCID 176—
Produkt1-(7-Fluoro-1H-indol-3-yl)-N,N-dimethylmethanamineHCID 2490512974%

Reaktionsschritte

To a mixture of acetic acid (13.6 mL) and formaldehyde (0.340 mL, 4.5 mmol, 37% solution) under argon was added dimethyl amine (2.05 mL, 16.3 mmol., 40% solution). The reaction mixture was stirred for 10 min and then treated with 7-fluoroindole (540 mg, 4.0 mmol.). The resulting mixture was stirred at room temperature for ˜16 h. The reaction mixture was first neutralized with K2CO3 and then basified with NaOH (2N), and then extracted in ethyl acetate, washed with water, dried, and concentrated. Solid obtained was recrystallized from ethyl acetate and hexane to give (7-Fluoro-1H-indol-3-ylmethyl)dimethylamine (570 mg, 74%): mp 133-137° C., 1H NMR (500 MHz, CDCl3): 2.31 (s, 6H), 3.62 (s, 2H), 6.88-6.92 (dd, J=8.0 and 8.0 Hz, 1H), 7.00-7.04 (m, 1H), 7.16 (d, J=2.5 Hz, 1H), 7.46 (d, J=8.0 Hz, 1H), 8.34 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07491743B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-05c7c956e2f84f86b559b2a3c884a46a
Quellennotizuspto-grants-2009_02