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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168910Generated: October 26, 2026

Ammonium Hydroxide → 2-(Pyridin-3-yloxy)ethanamine

https://huagongshe.com/reaction/1168910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(2-Chloroethoxy)pyridineHCID 19957946—
SolventMethanolHCID 887—
Product2-(Pyridin-3-yloxy)ethanamineHCID 979379336.2%

Reaction Conditions

Temperature125 °C

Reaction Steps

The 2-chloro-1-(3-pyridyloxy)ethane (1.23 g, 7.80 mmol) was dissolved in methanol (25 mL) and added to concentrated ammonium hydroxide solution (29.7%, 14.8 M, 55 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 125° C. (oil bath temperature) for 42 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (10 mL) was added to the residue, and the solution (pH 6) was extracted with ether (3×25 mL) to remove impurities. The aqueous layer was diluted with saturated NaCl solution (15 mL) and basified to pH 12 with 10% NaOH solution (5 mL). The mixture was extracted with chloroform (4×50 mL). The combined light-yellow chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 0.390 g (36.2%) of a light-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627648B1
Source datasetuspto-grants-2003_09
ORD IDord-eb3d74b1be01492cb0f8ecaa5adab776
Source noteuspto-grants-2003_09