Piperidine → HCID 22048494, compound

Participants

Reaction Steps

In an autoclave of 100 mL, piperidine (40.0 g, 470 mmol) was made reacted with chloroethyl methyl ether (22.0 g, 232 mmol) at 130 deg C. for 48 hours. Solid salt that was formed was removed by filtration, and residue (filtrate) was subjected to reduced-pressure distillation by using a Vigreux column of 25 cm. Then 1H-NMR measurement of obtained amine is performed, and it was confirmed that chemical shifts, δ (ppm), are 3.49-3.46 (t, 2H), 3.31(s, 3H), 2.51-2.48(t, 2H), 2.40-2.36(m, 4H), 1.59-1.53(m, 4H), and 1.42-1.36(m, 2H), and that N-2-methoxyethylpiperidine was synthesized.

Provenance & Evidence