Dethiation of α-methyl and α-phenylmercaptopropionic acid derivatives was written by Hannoun, Mohammad. And the article was included in Megallat Gamiat Al-Nagah Al-Abhat, A: Al-Ulum Al-Tabiiyyat in 2002.Category: alcohols-buliding-blocks This article mentions the following:
Dethiation of α-(3-benzoylphenyl)-α-Me and α-phenylmercaptopropionic acid with Raney nickel gave 2-(3-benzoylphenyl)propionic acid (20%), 2-[(3-α-hydroxybenzyl)phenyl]propionic acid (46%) and 2-(3-benzylphenyl)propionic acid (18%), resp. In the experiment, the researchers used many compounds, for example, 2-(3-(Hydroxy(phenyl)methyl)phenyl)propanoic acid (cas: 59960-32-6Category: alcohols-buliding-blocks).
2-(3-(Hydroxy(phenyl)methyl)phenyl)propanoic acid (cas: 59960-32-6) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Category: alcohols-buliding-blocks
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts