A Facile Method for Deprotection of O-Allylphenols using Palladium Charcoal
-
- Hayashida Maiko
- Tokyo University of Science
-
- Nishitani Kiyoshi
- Tokyo University of Science
-
- Hara Hiroshi
- Tokyo University of Science
-
- Ishizaki Miyuki
- Josai International University
Bibliographic Information
- Other Title
-
- O-アリルフェノールのパラジウム-炭素による簡便な脱アリル化
Description
We have investigated a new mild deprotective method for various O-allylphenols to give the corresponding phenols. The reaction of O-allylphenols bearing electron-withdrawing and weak electron-donating groups on the benzene ring proceeded smoothly, whereas the reaction of O-allylphenols having strong electron-donating groups gave phenols in nil to moderate yields. Mono-deprotection of O,O'-diallylcatechols was proceeded successfully to afford the corresponding O-allyloxyphenols. Moreover, we revealed that the present reaction proceeded via the SET process. Because 10% Pd/C is a heterogeneous catalyst, the deprotected phenol was obtained in essentially pure form by simple filtration and extraction procedure.
Journal
-
- Proceedings of the Symposium on Progress in Organic Reactions and Syntheses
-
Proceedings of the Symposium on Progress in Organic Reactions and Syntheses 31 (0), 260-260, 2005
Division of Organic Chemistry, The Pharmaceutical Society of Japan
- Tweet
Details 詳細情報について
-
- CRID
- 1390282680611154432
-
- NII Article ID
- 130006996771
-
- Data Source
-
- JaLC
- CiNii Articles
-
- Abstract License Flag
- Disallowed