30727-09-4

Usage

Uses

Used in Epoxy Resin Systems:
Tetrahydrofurfuryl-N,N-dimethylamine is used as a curing agent for epoxy resin systems, providing good mechanical and thermal resistance. Its properties make it suitable for a variety of industrial applications where durability and stability are required.
Used in Corrosion Inhibition:
In the industry, tetrahydrofurfuryl-N,N-dimethylamine serves as a corrosion inhibitor for metal surfaces, protecting them from degradation and extending their service life.
Used as a Catalyst:
tetrahydrofurfuryl-N,N-dimethylamine is also utilized as a catalyst in chemical reactions, facilitating processes and improving efficiency in various manufacturing and production settings.
Used in Various Formulations:
Due to its versatility, tetrahydrofurfuryl-N,N-dimethylamine is employed as an additive in a range of formulations across different industries, enhancing the performance of products and processes.

InChI:InChI=1/C7H15NO/c1-8(2)6-7-4-3-5-9-7/h7H,3-6H2,1-2H3

Upstream product

• 109-99-9 tetrahydrofuran 
• 50-00-0 formaldehyd 
• 124-40-3 dimethyl amine 
• 14496-34-5 (furan-2-ylmethyl)dimethylamine 
• 98-01-1 furfural 

Relevant academic research and scientific papers

A free radical Mannich type reaction: selective α-CH aminomethylation of ethers by Ti(III)/t-BuOOH system under aqueous acidic conditions

tert-Butoxy radical, generated by Ti(III)-one electron reduction of tert-butylhydroperoxide, selectively abstracts an α-H atom from ethers. The resulting α-ethereal radicals add to the C-atom of methylene iminium salts, formed in situ under aqueous acidic conditions, leading to a one-pot aminomethylation of ethers at room temperature. The aminoalkylation of ethers is also considered and the role of the metal ion is discussed.

N,N-dimethyl tetrahydrofurfuryl amine synthesis method

The invention relates to organic compound synthesis methods, in particular to an N,N-dimethyl tetrahydrofurfuryl amine synthesis method. The method includes steps: 1) mixing reactants with N,N-dimethyl formamide or N,N-dimethylacetamide and formic acid in a reaction vessel, and performing heating reaction; 1) after heating reaction is finished, performing distillation recovery of DMF (dimethyl formamide) or DMAC (dimethylacetamide) and the formic acid, and subjecting residues to vacuum distillation to obtain N,N-dimethyl furfuryl amine which is an intermediate product; 3) subjecting the intermediate product N,N-dimethyl furfuryl amine to catalytic hydrogenation, and distilling to obtain a product of N,N-dimethyl tetrahydrofurfuryl amine. The N,N-dimethyl tetrahydrofurfuryl amine synthesis method has advantages that raw materials are cheap and extensive in source; problems of low furfural yield and difficulty in separation due to instability of furfural acids are avoided, and acidity and reducibility of the formic acid are fully used; high hydrogenation selectivity and catalyst recyclability are realized; mild conditions, easiness in implementation and high raw material utilization rate are realized, and excessive formic acid and N,N-dimethyl formamide or N,N-dimethylacetamide are easy to recover.