4385-05-1Relevant articles and documents
Preparation method of 4-(2-(N, N-dimethylamino)ethyl)morpholine
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Paragraph 0030-0054, (2021/01/24)
The invention discloses a preparation method of 4-(2-(N, N-dimethylamino)ethyl)morpholine in the technical field of organic synthesis chemical industry, which comprises the following steps: dissolving2, 2'-diethylene glycol sulfonate and N, N-dimethylethylenediamine used as initial raw materials in a solvent, and carrying out cyclization reaction in the presence of an acid-binding agent to prepare 4-(2-(N, N-dimethylamino)ethyl)morpholine, the acid-binding agent is one of triethylamine, sodium hydroxide, sodium bicarbonate, sodium carbonate and potassium carbonate, the solvent is one of dimethyl sulfoxide, N, N-dimethyl formamide, N, N-dimethyl acetamide and tetrahydrofuran, the reaction temperature is 60 DEG C to 80 DEG C, and the reaction time is 6-9 hours. The method is mild in reaction condition and simple to operate, and has good popularization and application values, the obtained target product has huge application value in the aspects of chemical pharmacy, pesticides, organic synthesis and the like.
Well-Defined Phosphine-Free Iron-Catalyzed N-Ethylation and N-Methylation of Amines with Ethanol and Methanol
Lator, Alexis,Gaillard, Sylvain,Poater, Albert,Renaud, Jean-Luc
supporting information, p. 5985 - 5990 (2018/10/02)
An iron(0) complex bearing a cyclopentadienone ligand catalyzed N-methylation and N-ethylation of aryl and aliphatic amines with methanol or ethanol in mild and basic conditions through a hydrogen autotransfer borrowing process is reported. A broad range of aromatic and aliphatic amines underwent mono- or dimethylation in high yields. DFT calculations suggest molecular hydrogen acts not only as a reducing agent but also as an additive to displace thermodynamic equilibria.