Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305716Generated: October 25, 2026

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

https://huagongshe.com/reaction/2305716

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 100% 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 numberUS06441006B2
Source datasetuspto-grants-2002_08
ORD IDord-e732b8bb2c27456f962b497cda1fec6f
Source noteuspto-grants-2002_08