2-Substituted 1,3-propanediols as extractants of boric acid was written by Bernane, A.;Svarcs, E.;Timoteus, H.;Hansens, T.. And the article was included in Latvijas PSR Zinatnu Akademijas Vestis, Kimijas Serija in 1987.Product Details of 115-84-4 The following contents are mentioned in the article:
The distribution of H3BO3 in the organic and aqueous phases in extraction by diisobutyl-1,3-propanediol, 2-octyl-1,3-propanediol, 2-ethyl-2-butyl-1,3-propanediol, and 1-(3-bromophenyl)-2,2-dimethyl-1,3-propanediol was studied. The effects of diluents (HCCl3, PhMe, acetophenone, isoamyl alc., C2Cl4, decyl alc.) and salting out agents (NaCl, KCl, MgSO4, MgCl2) in H3BO3 extraction were determined The extraction effectiveness of the substituted propanediols was closely similar. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Product Details of 115-84-4).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Product Details of 115-84-4
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts