Ambartsumova, R. F. published the artcileOn interaction of 2-aminobenzothiazoles with halohydrins, Application of 1-Bromo-3-(3-bromopropoxy)propane, the main research area is benzothiazolamine halohydrin alkylation oxidation dimerization; iminobenzothiazoline preparation; benzothiazolylideneammonium chloride preparation.
On heating on a boiling water bath, 2-aminobenzothiazoles react with Cl(CH2)2OH to yield mainly the corresponding 3-(2-chloroethyl)benzothiazolin-2-ones. Reducing the reaction temperature increases the fraction of 2-imino-3-(2-hydroxyethyl)benzothiazolines. In both instances, formation of bis[3-(2-hydroxyethyl)benzothiazol-2-ylidene]ammonium chlorides is observed The reaction of 2-aminobenzothiazole with Br(CH2)3OH gives only the corresponding amino alcs. The anomalous products from the reaction of β-chloroethyl derivatives of benzothiazolinones result from a dominating side-reaction of the starting 2-aminobenzothiazoles with the Cl(CH2)2OH thermolysis products that are formed on boiling.
Chemistry of Heterocyclic Compounds (New York)(Translation of Khimiya Geterotsiklicheskikh Soedinenii) published new progress about Halohydrins Role: RCT (Reactant), RACT (Reactant or Reagent). 58929-72-9 belongs to class bromides-buliding-blocks, name is 1-Bromo-3-(3-bromopropoxy)propane, and the molecular formula is C6H12Br2O, Application of 1-Bromo-3-(3-bromopropoxy)propane.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary