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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168952Generated: November 1, 2026

Methylamine → HCID 10176377, compound

https://huagongshe.com/reaction/1168952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 22989732HCID 22989732—
SolventMethanolHCID 887—
ProductHCID 10176377HCID 1017637745.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

The 3-chloro-1-(6-methyl(3-pyridyloxy))propane (2.78 g, 18.3 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 was adjusted to 1 with 10% HCl solution and impurities were extracted with chloroform (4×25 mL). The pH of the aqueous phase was raised to 7 with 10% NaOH solution and other impurities were extracted with ether (4×30 mL). The aqueous layer was basified to pH 11 with 10% NaOH solution and extracted with ether (4×50 mL). The combined ether extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 1.224 g (45.3%) of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627648B1
Source datasetuspto-grants-2003_09
ORD IDord-424df4fd0ed0408b94037075244a37a1
Source noteuspto-grants-2003_09