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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168949Generated: October 25, 2026

Methylamine → Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine

https://huagongshe.com/reaction/1168949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant5-(3-Chloropropoxy)-3-(phenylmethoxy)pyridineHCID 22989698—
SolventMethanolHCID 887—
ProductMethyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amineHCID 988195371.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

The 5-(3-chloropropoxy)-3-(phenylmethoxy)pyridine (1.52 g, 5.49 mmol) was dissolved in methanol (25 mL) and added to a 40 wt % aqueous solution of methylamine (50 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 100° C. (oil bath temperature) for 4 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (25 mL) was added to the residue. The pH of the solution was adjusted to 6, and impurities were extracted with ether (3×15 mL). The aqueous layer was basified to pH 10 with 10% NaOH solution and extracted with chloroform (4×15 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 1.07 g (71.7%) of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627648B1
Source datasetuspto-grants-2003_09
ORD IDord-3f8d37cf7c974bdf8e7c5cf9d164df54
Source noteuspto-grants-2003_09