HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305722Generated: November 1, 2026
Ethylamine → Ethyl(3-(3-pyridyloxy)propyl)amine
https://huagongshe.com/reaction/2305722
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 3-(3-Chloro-propoxy)-pyridine | HCID 18433343 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl(3-(3-pyridyloxy)propyl)amine | HCID 9877539 | 38.1% |
Reaction Steps
The 3-chloro-1-(3-pyridyloxy)propane (1.00 g, 5.84 mmol) was dissolved in methanol (50 mL) and added to a 2.0 M solution of ethylamine in tetrahydrofuran (5 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 400 mg (38.1%) of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06441006B2 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-d9eafff77a844611aa285e57205dc0a6 |
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| Source note | uspto-grants-2002_08 |
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