The Phototransposition in Acetonitrile and the Photoaddition of 2,2,2-Trifluoroethanol to the Six Isomers of Dimethylbenzonitrile
The six dimethylbenzonitriles can be divided into two independent triads in their photochemical reactivity. The first triad is comprised of the 2,3-dimethyl, 3,4-dimethyl, and 2,6-dimethyl isomers (11 - 2,3, 11 - 3,4, and 11 - 2,6, respectively); the second triad is comprised of the 2,4-dimethyl, 2,...
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| Published in: | Journal of organic chemistry Vol. 65; no. 19; pp. 6173 - 6178 |
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| Main Authors: | , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
American Chemical Society
22-09-2000
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| Online Access: | Get full text |
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| Summary: | The six dimethylbenzonitriles can be divided into two independent triads in their photochemical reactivity. The first triad is comprised of the 2,3-dimethyl, 3,4-dimethyl, and 2,6-dimethyl isomers (11 - 2,3, 11 - 3,4, and 11 - 2,6, respectively); the second triad is comprised of the 2,4-dimethyl, 2,5-dimethyl, and 3,5-dimethyl isomers (11 - 2,4, 11 - 2,5, and 11 - 3,5, respectively). In acetonitrile, phototransposition converts the members of one triad to other members of the same triad, although only 11 - 3,4 was reactive enough to have significant conversion approaching a steady-state composition. Irradiation in 2,2,2-trifluoroethanol (TFE) resulted in the formation of addition products, 6-cyano-X,Y-dimethylbicyclo[3.1.0]hex-3-en-2-yl 2,2,2,-trifluoroethyl ethers, but in significant yield only from 11 - 3,4 of the first triad and 11 - 2,4 of the second triad. The 11 - 3,4 isomer gave seven major regio- and stereoisomers; the 11 - 2,4 isomer gave three different regio- and stereoisomers. These addition products were all explained by formation of bicyclo[3.1.0]hex-3-en-1-yl cations resulting from protonation by TFE at C6 followed by nucleophilic trapping by TFE. From these and previous results on aromatic nitriles, a consistent mechanistic picture is obtained where the critical carbon in determining the products of the phototransposition and photoaddition reactions is the cyano substituted one. |
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| Bibliography: | ark:/67375/TPS-0Z2ZXJFW-J istex:5749B9683BB8C1A855024C15FEDF720A7C5A88BC ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 0022-3263 1520-6904 |
| DOI: | 10.1021/jo000701e |