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	<title>Comments on: Mono N-methylation</title>
	<atom:link href="http://pmgb.wordpress.com/2008/03/26/mono-n-methylation/feed/" rel="self" type="application/rss+xml" />
	<link>http://pmgb.wordpress.com/2008/03/26/mono-n-methylation/</link>
	<description>chemical reaction procedures</description>
	<lastBuildDate>Tue, 10 Nov 2009 16:18:40 +0000</lastBuildDate>
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		<title>By: pmgb</title>
		<link>http://pmgb.wordpress.com/2008/03/26/mono-n-methylation/#comment-34</link>
		<dc:creator>pmgb</dc:creator>
		<pubDate>Tue, 08 Apr 2008 17:05:20 +0000</pubDate>
		<guid isPermaLink="false">http://pmgb.wordpress.com/?p=34#comment-34</guid>
		<description>Ref: 
1.http://designer-drugs.com/pte/12.162.180.114/dcd/chemistry/amphetamine.methylation.html
 and the references there in
2. http://www.alsnotebook.com/reductalk.html (procedure and mechanism)
3. Bhattacharyya, S. Synth. Commun. 1995, 25, 2061-2069.

We need the monomethylated product which cannot be accessed by using methyl iodide (overmethylation takes place).
Hydrogenation (Pd-C, H2) can also be used to reduce the imine intermediate (see Al&#039;s notebook). </description>
		<content:encoded><![CDATA[<p>Ref:<br />
1.http://designer-drugs.com/pte/12.162.180.114/dcd/chemistry/amphetamine.methylation.html<br />
 and the references there in<br />
2. <a href="http://www.alsnotebook.com/reductalk.html" rel="nofollow">http://www.alsnotebook.com/reductalk.html</a> (procedure and mechanism)<br />
3. Bhattacharyya, S. Synth. Commun. 1995, 25, 2061-2069.</p>
<p>We need the monomethylated product which cannot be accessed by using methyl iodide (overmethylation takes place).<br />
Hydrogenation (Pd-C, H2) can also be used to reduce the imine intermediate (see Al&#8217;s notebook).</p>
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	<item>
		<title>By: J.R</title>
		<link>http://pmgb.wordpress.com/2008/03/26/mono-n-methylation/#comment-33</link>
		<dc:creator>J.R</dc:creator>
		<pubDate>Tue, 08 Apr 2008 09:59:39 +0000</pubDate>
		<guid isPermaLink="false">http://pmgb.wordpress.com/?p=34#comment-33</guid>
		<description>what is your reference for the quote ......is there a problem with more than mono methylation of the amine?  It&#039;s assumed also that hydrogenation of the material with Pd as a catalyst will also give the desired mono methylated amine....?</description>
		<content:encoded><![CDATA[<p>what is your reference for the quote &#8230;&#8230;is there a problem with more than mono methylation of the amine?  It&#8217;s assumed also that hydrogenation of the material with Pd as a catalyst will also give the desired mono methylated amine&#8230;.?</p>
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