Abstract
An efficient method for preparation of 3-formyl-2-arylbenzo[b]furan derivatives 4 from 3-chloro-2-(2-methoxyaryl)-1-arylprop-2-en-1-one 2 was developed, and the desired product was obtained in good to excellent yields. By converting 2-(2-methoxyphenyl)-3-oxo-3-phenylpropanal 1 to 2, the regioselectivity problem occurring in the reaction when using 1 as the starting material was successfully avoided. Furthermore, a one-pot procedure for the successive demethylation, cyclization, and hydrolysis was evolved, although the intermediate 3-(dibromomethyl)-2-phenylbenzo[b]furan 3a could be isolated. A plausible mechanism was proposed based on some in situ investigations.
| Original language | English |
|---|---|
| Pages (from-to) | 3274-3277 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 55 |
| Issue number | 21 |
| DOIs | |
| State | Published - 21 May 2014 |
Keywords
- 3-Formyl-2-arylbenzo[b]furan
- Cyclization reaction
- Demethylation reaction
- Vinyl chloride