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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33701Generated: October 28, 2026

Potassium Iodide → Ammonia methanol

https://huagongshe.com/reaction/33701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPiperidineHCID 8082—
ReactantSodium CarbonateHCID 10340—
Reactant3-Chloropropyl 4-(piperidinomethyl)phenyl etherHCID 4365932—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
Product1-(3-(4-(1-Piperidinylmethyl)phenoxy)propyl)piperidineHCID 2766326—
ProductAmmonia methanolHCID 217058975%

Reaction Steps

A solution of the product of Example 12 (6.13 g), piperidine (3.0 mL), sodium carbonate (3.6 g), and potassium iodide (190 mg) in n-butanol (50 mL) was heated to 105° C. for 21 h, cooled to RT, and treated with water (50 mL). The resulting mixture was extracted with DCM (4×50 mL), and the combined organic phases were dried (magnesium sulfate) and evaporated. Chromatography of the residue (5% 2M methanolic ammonia/methanol) gave the title compound as a waxy solid (3.2 g). 1H NMR (400 MHz, CDCl3): 7.19 (d, J=8.6 Hz, 2H), 6.83 (d, J=8.8 Hz, 2H), 3.97 (t, J=6.5 Hz, 2H), 3.4 (s, 2H), 2.48-2.31 (m, 10H), 2.00-1.92 (m, 2H), 1.62-1.52 (m, 8H), 1.47-1.38 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429586B2
Source datasetuspto-grants-2008_09
ORD IDord-a08c5bdb0a6f4983863ec5dec4cade4b
Source noteuspto-grants-2008_09