18366-44-4

Usage

Uses

1-Propanol, 3-[(1,1-dimethylethyl)amino]is used as a component in the preparation of liquid waste gas desulfurization agents for the removal of organic and inorganic sulfur (S) from gases. These gases can include natural gas, coal gas, biogas, industrial waste gas, and refinery gas. The application reason for using 1-Propanol, 3-[(1,1-dimethylethyl)amino]- is its ability to effectively react with and remove sulfur compounds, which are harmful pollutants that contribute to air pollution and acid rain.
Used in Environmental Protection Industry:
1-Propanol, 3-[(1,1-dimethylethyl)amino]is used as a key component in the development of desulfurization agents for the environmental protection industry. Its role in this application is to facilitate the removal of sulfur-containing compounds from various gas sources, thereby reducing the environmental impact of these emissions and improving air quality.
Used in Industrial Gas Treatment:
In the industrial gas treatment sector, 1-Propanol, 3-[(1,1-dimethylethyl)amino]is utilized as an essential ingredient in the formulation of desulfurization agents. These agents are employed to treat gases produced during various industrial processes, ensuring that harmful sulfur compounds are removed before the gases are released into the atmosphere. This application helps in meeting environmental regulations and reducing the overall sulfur emissions from industrial activities.

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 761, 1994 DOI: 10.1016/S0040-4039(00)75811-4

Upstream product

• 1462-98-2 ethyl 3-(tert-butylamino)propanoate 
• 75-64-9 tert-butylamine 
• 627-30-5 1-chloro-3-hydroxypropane 
• 627-18-9 1-bromo-3-propanol 
• 21539-55-9 methyl 3-(N-tert-butylamino)propanoate 
• 503-30-0 trimethylene oxide 
• 169269-01-6 tert-Butyl-(3-hydroxy-propyl)-carbamic acid tert-butyl ester 
• 16486-68-3 N-allyl(tert-butyl)amine 
• 22675-81-6 N-(tert-butyl)propan-1-amine 
• 169268-94-4 Allyl-tert-butyl-carbamic acid tert-butyl ester 
• 71970-55-3 3-tert-butylamino-acrylaldehyde 

Downstream Products

• 130613-90-0 2-Benzyl-3-tert-butyl-[1,3,2]oxazaphosphinane 2-oxide 

Relevant academic research and scientific papers

Platinum-Catalyzed, Terminal-Selective C(sp3)-H Oxidation of Aliphatic Amines

This Communication describes the terminal-selective, Pt-catalyzed C(sp3)-H oxidation of aliphatic amines without the requirement for directing groups. CuCl2 is employed as a stoichiometric oxidant, and the reactions proceed in high yield at Pt loadings as low as 1 mol%. These transformations are conducted in the presence of sulfuric acid, which reacts with the amine substrates in situ to form ammonium salts. We propose that protonation of the amine serves at least three important roles: (i) it renders the substrates soluble in the aqueous reaction medium; (ii) it limits binding of the amine nitrogen to Pt or Cu; and (iii) it electronically deactivates the C-H bonds proximal to the nitrogen center. We demonstrate that this strategy is effective for the terminal-selective C(sp3)-H oxidation of a variety of primary, secondary, and tertiary amines.

N-t-butoxycarbonyl protection of primary and secondary amines in the hydroboration reaction: Synthesis of amino alcohols

The use of the BOC group as a protecting group in the hydroboration of aminoalkenes is described. The isolated yields of amino alcohols via the hydroboration-oxidation sequence are excellent.

Mild LIBF4-Promoted Aminolysis of Oxetanes

LiBF4 in acetonitrile efficiently catalyzes the aminolysis of trimethylene oxide and 2-octyl oxetane under mild conditions (r.t. or 80 deg C) to give the corresponding γ-amino alcohols in very good yields.

The Conformational Analysis of Saturated Heterocycles. Part 100. 1-Oxa-3-azacyclohexanes

Conformational equilibria and barriers to ring and nitrogen inversion are determined by 1H and 13C n.m.r. for 13 1-oxa-3-azacyclohexanes and correlated with recent work on the conformational analysis of saturated heterocycles.