N-(Phenylselenomethyl)phthalimide as new reagent for mild protection of alcohols as Pim-ethers was written by Temperini, Andrea;Minuti, Lucio. And the article was included in Tetrahedron Letters in 2012.Reference of 94022-96-5 This article mentions the following:
A mild activation of N-(phenylselenomethyl)phthalimide by iodonium ion in the presence of alcs. to give the corresponding O-phthalimidomethyl derivatives (Pim-ethers) I [R = t-Bu, cyclohexyl, O2NCH2CH2, etc.] is provided. Simple cleavage of the phthalimido group with ethylenediamine is also reported thus making this approach a new and efficient method of protecting alcs. In the experiment, the researchers used many compounds, for example, 2-(Trifluoromethyl)phenethyl alcohol (cas: 94022-96-5Reference of 94022-96-5).
2-(Trifluoromethyl)phenethyl alcohol (cas: 94022-96-5) 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. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Reference of 94022-96-5
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts