| Abstract: | The products formed in the oxidation of 2,6-di-tert-butyl-4-methylphenol with oxygen and sodium hydroxide at about 100?? are 3,5-di-tert-butyl-4-hydroxybenzaldehyde, trimethylacetic acid, an acidic compound C14H22O3, and probably 2,6-di-tert-butylbenzoquinone (which was actually isolated in the similar oxidation of the above-named benzaldehyde), in addition to compounds previously reported. Some of the properties of C14H22O3 are given, and the oxidation of it to 2,3-di-tert-butylsuccinic anhydride is described, but assignment of structure is reserved pending the completion of more experimental work. |
| Genre: | Article |
| ProdID: | 70010478 |
| Citation Author: | Yohe, G. R.; Dunbar, J. E.; Pedrotti, R. L.; Scheidt, F. M.; Lee, F. G. H.; Smith, E. C. |
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| Citation End Page: | 1292 |
| Citation Issue: | 11 |
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| Citation Language: | English |
| Citation Larger Work Title: | Journal of Organic Chemistry |
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| Citation Number Of Pages: | 4 |
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| Citation Publisher: | American Chemical Society |
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| Citation Search Results Text: | The oxidation of 2,6-di-tert-butyl-4-methylphenol; 1956; Article; Journal; Journal of Organic Chemistry; Yohe, G. R.; Dunbar, J. E.; Pedrotti, R. L.; Scheidt, F. M.; Lee, F. G. H.; Smith, E. C. |
| Citation Start Page: | 1289 |
| Citation Volume: | 21 |
| Citation Year: | 1956 |
| Type: | citation/reference |
| Text: | The oxidation of 2,6-di-tert-butyl-4-methylphenol; 1956; Article; Journal; Journal of Organic Chemistry; Yohe, G. R.; Dunbar, J. E.; Pedrotti, R. L.; Scheidt, F. M.; Lee, F. G. H.; Smith, E. C. |
| URL (THUMBNAIL): | http://pubs.er.usgs.gov/thumbnails/outside_thumb.jpg |
| URL (DIGITAL OBJECT IDENTIFIER): | http://dx.doi.org/10.1021/jo01117a020 |
| Date Other: | Sun, 1 Jan 1956 00:00 -0600 |
| Publisher: | American Chemical Society |
