Abstract
A method for the preparation of methyl 4-hydroxy-2-(trifluoromethyl)-4H- chromenes-3-carboxylate derivatives 3a-j from readily available trifluoromethylated building block methyl (Z)-2-bromo-4,4,4-trifluoro-2- butenoate 1 was described. Treatment of 3a-j with Sarrett reagent in CH 2Cl2 generated methyl 4-oxo-2-(trifluoromethyl)-chromene- 3-carboxylate derivatives 4a-h with moderate to good yields, which can be converted to 2-trifluoromethyl-substituted multifunctional benzoxepins through cyclopropanation and Lewis acid-catalyzed ring opening.
| Original language | English |
|---|---|
| Pages (from-to) | 171-177 |
| Number of pages | 7 |
| Journal | Journal of Fluorine Chemistry |
| Volume | 133 |
| DOIs | |
| State | Published - Jan 2012 |
| Externally published | Yes |
Keywords
- Chromene
- Chromones
- Oxa-Michael-aldol
- Trifluoromethyl
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