Abstract
A procedure for the continuous flow generation of thiomorpholine in a two-step telescoped format was developed. The key step was the photochemical thiol-ene reaction of cysteamine hydrochloride and vinyl chloride as low-cost starting materials under highly con-centrated (4 M) conditions, leading to the corresponding half-mustard intermediate in quantitative yield. Thiomorpholine was subsequently obtained by a base-mediated cyclization. The robust-ness of the process was demonstrated by performing the reaction for 7 h (40 min overall residence time) isolating the desired thio-morpholine via distillation.
Supplementary materials
Title
Synthesis of Thiomorpholine via a Telescoped Photochemical Thiol-ene/Cyclization Sequence in Continuous Flow
Description
Additional experimental details, photographs of reactor set-up, further optimizations studies, 1H NMR and 13C NMR spectra
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