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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098612Generated: October 27, 2026

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

https://huagongshe.com/reaction/1098612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant7-Fluoro-1H-indoleHCID 2774504—
SolventAcetic AcidHCID 176—
Product1-(7-Fluoro-1H-indol-3-yl)-N,N-dimethylmethanamineHCID 2490512974%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143300B2
Source datasetuspto-grants-2012_03
ORD IDord-554ffaa698dc49f989831814a088d201
Source noteuspto-grants-2012_03