The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (2S)-(+)-3-Chloropropane-1,2-diol( cas:60827-45-4 ) is researched.Quality Control of (2S)-(+)-3-Chloropropane-1,2-diol.Iriuchijima, Shinobu; Kojima, Natsuko published the article 《Asymmetric hydrolysis of esters by biochemical methods. Part III. Asymmetric hydrolysis of (±)-1,2-diacetoxy-3-chloropropane and its related compounds with lipase. Synthesis of optically pure (S)-propranolol》 about this compound( cas:60827-45-4 ) in Agricultural and Biological Chemistry. Keywords: diacetoxychloropropane asym hydrolysis lipase. Let’s learn more about this compound (cas:60827-45-4).
Asym. hydrolysis of (±)-1,2-diacetoxy-3-chloropropane (I) using lipoprotein lipase gave (S)-I of 90% enantiomeric excess (e.e.). Reactions of (S)-I with phenols in an alk. condition yielded the corresponding (S)-3-aryloxy-1,2-propranediols. (S)-Propranolol was prepared from (S)-3-(1-naphthoxy)-1,2-propanediol. Hydrolysis of (±)-1,2-diacetoxy-3-bromopropane (II) and (±)-1,2-diacetoxyethylbenzene (III) with the lipase afforded (S)-II of 77% e.e. and (R)-III of 73% e.e., resp.
As far as I know, this compound(60827-45-4)Quality Control of (2S)-(+)-3-Chloropropane-1,2-diol can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com