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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-(2-Chloroethoxy)pyridine | HCID 19957946 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Pyridin-3-yloxy)ethanamine | HCID 9793793 | 36.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627648B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-eb3d74b1be01492cb0f8ecaa5adab776 |
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| Source note | uspto-grants-2003_09 |
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