FeCl3 as an efficient and new catalyst for the thia-Fries rearrangement of aryl sulfinates
β Scribed by Firouz Matloubi Moghaddam; Mohammad G Dekamin; Mohammad Ghaffarzadeh
- Book ID
- 104231783
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 55 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Aryl arenesulfinates rearrange to the corresponding arenesulfinyl phenols via a thia-Fries rearrangement on catalysis by anhydrous FeCl 3 in dry dichloromethane at room temperature in good to excellent yields.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A new facile method for direct sulfonylation of phenols was developed. Graphite in methanesulfonic acid (GMA) was used to prepare sulfonylphenols by sulfonylation of phenol and naphthalene derivatives with __p__βtoluenesulfonic acid (=4βmethylbenzenesulfonic acid) (__Tableβ 1__) and the
## Abstract For Abstract see ChemInform Abstract in Full Text.