反应详情

A mixture of N-(p-chloro-a-cyanobenzyl)-2,2,2-trifluoroacetamide (10.5 g, 0.04 mol) and toluene is cooled to 5°-10° C. under a nitrogen atmosphere, treated with trifluoromethanesulfonic acid (12.0 g, 0.08 mol) over a 20 minute period, allowed to warm to room temperature and held at 25° C. for 3 hours. The formation of the intermediate 5-amino oxazole salt is monitored by 19F NMR (DMSO-d6). When the intermediate salt formation is complete, the mixture is cooled below 20° C., treated with dimethylformamide and 2-chloroacrylonitrile (5.25 g, 0.06 mol), held at 25° C. for 16-18 hours, and treated with ethyl acetate and water. The phases are separated and the organic phase is washed with water and concentrated in vacuo to give a solid residue. Flash column chromatography of the residue on silica gel, packed and eluted respectively with 15% and 20% ethyl acetate in heptane gives the title product as pale yellow crystals, 6.14 g (57% yield), mp 237°-240° C., identified by HPLC and NMR analyses.

1. temperatureis cooled to 5°-10° C. under a nitrogen atmosphere
2. temperaturethe mixture is cooled below 20° C.
3. waitheld at 25° C. for 16-18 hours
4. customThe phases are separated
5. washthe organic phase is washed with water
6. concentrationconcentrated in vacuo
7. customto give a solid residue
8. washeluted respectively with 15% and 20% ethyl acetate in heptane