Dihydroxyacetone (DHA) was obtained in good yield from the selective formose reaction which was conducted with 2-(dimethylamino)ethanol and vitamin B1 in N,N-dimethylformamide (DMF). The major products were isolated from the formose and identified as dihydroxyacetone and 2-(1,2-dihydroxyethyl)-5-(2-hydroxyethyl)-4-methylthiazole by spectral data. Vitamin B1 suppressed the vaporization of formaldehyde from the reaction solution. Irrespective of the 2-(dimethylamino)ethanol concentration (above 0.1 M (1M=1 mol dm−3)), the maximum yield of DHA was 80–90 glc% at 1.0 M formaldehyde concentration, when the formaldehyde consumption was above 90%. Above 3.0 M formaldehyde concentration, selective formation of DHA (above 80 glc%) was obtained at the early stage of the reaction. The scheme for the formation of DHA in the formose reaction in the presence of vitamin B1 was also proposed.
No takes yet. Share an insight, caveat, or question.
Shigemasa et al. (1984) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: