HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305701Generated: October 31, 2026
Methylamine → Methyl(4-(3-pyridyloxy)butyl)amine
https://huagongshe.com/reaction/2305701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Chloro-1-(3-pyridyloxy)butane | HCID 22989700 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl(4-(3-pyridyloxy)butyl)amine | HCID 9794054 | 75.5% |
Reaction Steps
The 4-chloro-1-(3-pyridyloxy)butane (2.00 g, 10.8 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 (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 basified to pH 10 with 100% NaOH solution, and the mixture was extracted with chloroform (4×25 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 1.47 g (75.5%) 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-6f66983fada8465f851f8fd911db6e01 |
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| Source note | uspto-grants-2002_08 |
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