Abstract
The reactions of propanal and pentanal with 2-(hydroxymethyl)piperidine were investigated by Fourier transform infrared spectrometry attenuated total reflectance in both the solution phase and at the gas/solid interface. The reactions were studied with the use of a flow-through cylindrical internal reflection ("circle") cell. Reaction intermediates were tentatively identified by their characteristic infrared absorption frequencies. At the gas/solid interface the reaction is thought to yield a hemiaminal intermediate. In the solution phase a hemiaminal intermediate is believed to form initially, followed by loss of water to generate an enamine product. In both gas-phase and solution-phase studies, an oxazolidine product is prepared only after an ultrasound treatment. The FT-IR/ATR technique reveals detailed mechanistic information concerning reactions between aldehydes and ethanol amines.
PDF Article
More Like This
Cited By
You do not have subscription access to this journal. Cited by links are available to subscribers only. You may subscribe either as an Optica member, or as an authorized user of your institution.
Contact your librarian or system administrator
or
Login to access Optica Member Subscription