1-Phenacyl-, 1-carbethoxymethyl- and 1-benzyl-4-dimethylaminopyridinium halides: Isolation and use for generating ylide
IR@NISCAIR: CSIR-NISCAIR, New Delhi - ONLINE PERIODICALS REPOSITORY (NOPR)
View Archive InfoField | Value | |
Creator |
Nallu, M
Sathiskumar, V Sangeetha, M K Sarkunam, K |
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Date |
2013-10-18T06:09:45Z
2013-10-18T06:09:45Z 2001-04 |
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Identifier |
0975-0983(Online); 0376-4699(Print)
http://hdl.handle.net/123456789/22238 |
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Description |
295-298
Active halide containing electron withdrawing group (EWG) α-to halogen readily reacts with 4-dimethylaminopyridine (DMAP) to give stable salt of pyridinium halide (<b>1-6</b>). The reaction between 1-phenacyl-4-dimethylaminopyridinium halide(s) (<b>1</b> and <b>2</b>) and aq. NaOH instantaneously generates 4-dimethylaminopyridinium-1-(2'-hydroxy-2'-phenyl)vinylide <b>7</b> as brownish yellow stable crystalline solid which is reported for the first time. Whereas, the other compounds <b>3-6</b> do not generate such type of ylide under identical experimental conditions. |
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Language |
en_US
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Publisher |
NISCAIR-CSIR, India
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Rights |
<img src='http://nopr.niscair.res.in/image/cc-license-sml.png'> <a href='http://creativecommons.org/licenses/by-nc-nd/2.5/in' target='_blank'>CC Attribution-Noncommercial-No Derivative Works 2.5 India</a>
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Source |
IJC-B Vol.40B(04) [April 2001]
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Title |
1-Phenacyl-, 1-carbethoxymethyl- and 1-benzyl-4-dimethylaminopyridinium halides: Isolation and use for generating ylide
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Type |
Article
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