(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.COA of Formula: C4H11NO
Specific cooperative effect for the enantiomeric separation of amino acids using aqueous two-phase systems with task-specific ionic liquids was written by Wu, Datong;Zhou, Ying;Cai, Pengfei;Shen, Shanshan;Pan, Yuanjiang. And the article was included in Journal of Chromatography A in 2015.COA of Formula: C4H11NO This article mentions the following:
Aqueous two-phase systems (ATPS) based on hydrophilic ionic liquid (IL) and inorganic salt solution were designed and prepared for the enantiomeric separation of racemic amino acids. Two different kinds of hydrophilic ionic liquids (I, IL-1 and II IL-2) containing functional groups were synthesized to sep. racemic amino acids. Preliminary experiments showed that D-enantiomer of amino acids cooperatively interacted with ILs, which pushed D-enantiomer to remain in the bottom IL-rich phase. By contrast, L-enantiomer was transferred into the top Na2SO4-rich phase. The enantioselectivity of IL-1 was better than that of IL-2 because of their different intermol. interactions. Various factors influencing separation efficiency were also systematically studied including extraction time, IL volume and temperature Also, the mechanism was studied by 1H NMR and DFT calculations, which showed that the hydrogen bond between the carboxylate and amide groups and the resonance-assisted hydrogen bond between amino and hydroxyl groups conditioned the movement between the residues and ILs. Finally, IL-1 was validated with other general amino acids by the same procedures based on ATPS. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3COA of Formula: C4H11NO).
(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.COA of Formula: C4H11NO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts