The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (2S)-(+)-3-Chloropropane-1,2-diol(SMILESS: OC[C@H](O)CCl,cas:60827-45-4) is researched.Category: iodides-buliding-blocks. The article 《A novel method for synthesis of L- and D-glycerol acetonide》 in relation to this compound, is published in Yingyong Huaxue. Let’s take a look at the latest research on this compound (cas:60827-45-4).
A novel efficient method for preparation. L- and D-glycerol acetonide is described. Highly enantioenriched (S)-epichlorohydrin and (R)-3-chloro-1,2-propanediol were simultaneously prepared by hydrolysis and resolution of racemic epichlorohydrin in presence of a chiral (R,R)-Salen-CoIII complex. (S)-epichlorohydrin was then used to afford L-glycerol acetonide in overall yield of 59.4 % by hydrolysis, condensation with acetone, substitution (acetylation), and alcoholysis. D-glycerol acetonide was prepared from (R)-3-chloro-1,2-propanediol in overall yield of 62.5 %. The chem. structures of the target compounds were confirmed by IR, 1H NMR and MS.
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Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com