Formula: C3H7ClO2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (2S)-(+)-3-Chloropropane-1,2-diol, is researched, Molecular C3H7ClO2, CAS is 60827-45-4, about Synthesis of highly enantiomerically enriched arenesulfonic acid 2-hydroxy esters via kinetic resolution of terminal epoxides. Author is Lee, Yae Won; Yang, Hee Chun; Kim, Geon-Joong.
This paper describes the very efficient and highly enantioselective ring opening of terminal epoxides with alkyl and arene sulfonic acid. The dinuclear chiral (salen) Co complexes bearing Lewis acids of Al, Ga and In catalyze the reaction enantioselectively in the presence of tetrabutylammonium chloride using tert-Bu Me ether as a solvent. The variation of the anion of the tetra Bu ammonium salt has significant impact on the reactivity and selectivity of the asym. ring opening of Ph glycidyl ether with p-toluenesulfonic acid. The order of reactivity and selectivity was found to be Cl- > l- > Br- > OH-. Strong synergistic effects of the different Lewis acid centers of Co-Al, Co-Ga and Co-In complexes were observed in the catalytic process. The dinuclear chiral salen catalyst containing AlCl3 was found to be most active and highly enantioselective (91% ee).
Although many compounds look similar to this compound(60827-45-4)Formula: C3H7ClO2, numerous studies have shown that this compound(SMILES:OC[C@H](O)CCl), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com