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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-Chloro-1-(3-pyridyloxy)butaneHCID 22989700—
SolventMethanolHCID 887—
ProductMethyl(4-(3-pyridyloxy)butyl)amineHCID 979405475.5%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441006B2
Source datasetuspto-grants-2002_08
ORD IDord-6f66983fada8465f851f8fd911db6e01
Source noteuspto-grants-2002_08