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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 5-(3-Chloropropoxy)-3-(phenylmethoxy)pyridine | HCID 22989698 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine | HCID 9881953 | 71.7% |
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
| 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-3f8d37cf7c974bdf8e7c5cf9d164df54 |
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| Source note | uspto-grants-2003_09 |
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