Bachelier, N. et al. published their research in Journal of Membrane Science in 1996 | CAS: 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. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 115-84-4

Facilitated transport of boric acid by 1,3-diols through supported liquid membranes was written by Bachelier, N.;Chappey, C.;Langevin, D.;Metayer, M.;Verchere, J.-F.. And the article was included in Journal of Membrane Science in 1996.Reference of 115-84-4 The following contents are mentioned in the article:

Boric acid is transported selectively by 1,3-diols from an aqueous source phase into an alk. aqueous receiving phase through an organic solvent (o-dichlorobenzene) phase. Measurements of the transport rates were made by using a U-tube apparatus The process was adapted to liquid membranes supported on polypropylene films. The factors which influence the stability of the supported liquid membrane are discussed. Assuming that the transport of the neutral 1:1 diol-boric acid complex within the organic phase is diffusion-limited, a model is proposed that realistically represents the fluxes of boric acid as a function of the initial concentrations of boric acid and diol. The exptl. diffusion coefficients were determined and agreed satisfactorily with the calculated values. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Reference 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. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Reference of 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts