From: Ravi Orugunty (rorugunty$##$oragenics.com)
Date: Thu Mar 09 2006 - 13:09:33 EST
Regarding separation of pyridine from ethanol.
Do you know the approximate ratio of the two compounds in the mixture? If
you do then add enough concentrated HCl or pass HCl gas thru the mixture.
This will form pyridine.HCl salt that will not distill out with ethanol.
You can recover the pyridine by neutralizing the HCl with NaOH and distill
it separately.
best of luck
ravi
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Today's Topics:
1. Re: NMR spectra (Etienne van Zyl)
2. Seperation of nitro compounds (srinivas reddy)
3. Separation of mixtures (fine chem)
4. Re: NMR spectra (Darren Rhodes)
5. RE: Separation of mixtures (Ilya Avrutov)
6. nitroarene reduction (diogo$##$unilavras.edu.br)
7. R'-OH --> R'-NH-R" (bijster bagger)
8. Re: Seperation of nitro compounds (Sengen Sun)
----------------------------------------------------------------------
Message: 1
Date: Wed, 8 Mar 2006 21:09:32 -0000
From: "Etienne van Zyl" <etiennevanzyl$##$tiscali.co.uk>
Subject: Re: ORGLIST: NMR spectra
To: "Sylvie Ducki" <sylvie_ducki$##$yahoo.com>, <ed.arruda$##$iff.com>
Cc: everybody$##$orglist.net, everybody-bounces$##$orglist.net
Message-ID: <005301c642f4$98836840$e2596d58$##$DELL20050128>
Content-Type: text/plain; format=flowed; charset="iso-8859-1";
reply-type=original
Sylvie
ACD Chemsketch 8.0 freeware is available at this site:
http://www.acdlabs.com/download/chemsk.html
Suitable for Proton and 13C prediction - it may help.
Etienne van Zyl
Oxfordshire
----- Original Message -----
From: <ed.arruda$##$iff.com>
To: "Sylvie Ducki" <sylvie_ducki$##$yahoo.com>
Cc: <everybody$##$orglist.net>; <everybody-bounces$##$orglist.net>
Sent: Tuesday, March 07, 2006 9:22 PM
Subject: Re: ORGLIST: NMR spectra
> Sylvie,
>
> I use the following websites occasionally.
>
> http://www2.chemie.uni-erlangen.de/services/spinus/
>
> http://www.nmrshiftdb.org/
>
> Hope it helps
>
> Ed Arruda
> Senior Scientist
> International Flavors and Fragrances
>
>
> _______________________________________________
> ORGLIST - Organic Chemistry Mailing List
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Message: 2
Date: Wed, 8 Mar 2006 17:38:23 -0800 (PST)
From: srinivas reddy <gounisrinivas$##$yahoo.com>
Subject: ORGLIST: Seperation of nitro compounds
To: everybody$##$orglist.net
Message-ID: <20060309013823.66297.qmail$##$web51807.mail.yahoo.com>
Content-Type: text/plain; charset=iso-8859-1
Hi,
can anybody help me on how to seperate the mixture of
aromatic nitro compounds that are formed by nitration
with HNO3/H2SO4?. I tried with column chromatography
but of not much use.
thanks in davance
GSR
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Message: 3
Date: Thu, 9 Mar 2006 04:40:32 -0800 (PST)
From: fine chem <chemicals555$##$yahoo.com>
Subject: ORGLIST: Separation of mixtures
To: everybody$##$orglist.net
Message-ID: <20060309124032.32916.qmail$##$web34203.mail.mud.yahoo.com>
Content-Type: text/plain; charset="iso-8859-1"
Dear All,
How can Ethanol be seperated from Pyridine, both in the same mix.
Fractional distillation yields a constant boiling point mixture of 75 deg
C
Thanks in advance.
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Message: 4
Date: Thu, 9 Mar 2006 13:04:11 +0000
From: "Darren Rhodes" <darren.rhodes$##$gmail.com>
Subject: Re: ORGLIST: NMR spectra
To: "everybody$##$orglist.net" <everybody$##$orglist.net>
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All ...
MestreC took as an input the FID data file from an NMR spectrum. The
software transformed this data from the time domain to the frequency
domain via the Fourier transform. The user could format the
subsequent NMR spectrum.
The suggestions thus far seem to miss this point. If you haven't used
MestreC you've missed out.
It was invaluable as a teaching aid.
It was invaluable for processing NMR FIDs that had been despatched by
email from an NMR provider.
It is tragic that the people at MestreC have gone down this line. Is
user pays the only business model for recouping money from software?
Wasn't there an open source Linux version called ... Swan NMR??? (Or
something????).
Darren.
On 3/8/06, Etienne van Zyl <etiennevanzyl$##$tiscali.co.uk> wrote:
> Sylvie
>
> ACD Chemsketch 8.0 freeware is available at this site:
> http://www.acdlabs.com/download/chemsk.html
>
> Suitable for Proton and 13C prediction - it may help.
>
> Etienne van Zyl
> Oxfordshire
>
>
>
>
> ----- Original Message -----
> From: <ed.arruda$##$iff.com>
> To: "Sylvie Ducki" <sylvie_ducki$##$yahoo.com>
> Cc: <everybody$##$orglist.net>; <everybody-bounces$##$orglist.net>
> Sent: Tuesday, March 07, 2006 9:22 PM
> Subject: Re: ORGLIST: NMR spectra
>
>
> > Sylvie,
> >
> > I use the following websites occasionally.
> >
> > http://www2.chemie.uni-erlangen.de/services/spinus/
> >
> > http://www.nmrshiftdb.org/
> >
> > Hope it helps
> >
> > Ed Arruda
> > Senior Scientist
> > International Flavors and Fragrances
> >
> >
> > _______________________________________________
> > ORGLIST - Organic Chemistry Mailing List
> > Website / Archive / FAQ: http://www.orglist.net
> > To post a message (TO EVERYBODY) send to everybody$##$orglist.net
> > To unsubscribe, send to everybody-request$##$orglist.net the message:
> > unsubscribe your_orglist_password your_address
> _______________________________________________
> ORGLIST - Organic Chemistry Mailing List
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unsubscribe your_orglist_password your_address
>
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Message: 5 Date: Thu, 9 Mar 2006 08:38:44 -0500 From: "Ilya Avrutov" <IAvrutov$##$dalton.com> Subject: RE: ORGLIST: Separation of mixtures To: "fine chem" <chemicals555$##$yahoo.com>, <everybody$##$orglist.net> Message-ID: <3C4E01DBE4138446A742AC296B57F30D463249$##$dalton-es.dalton.dcl> Content-Type: text/plain; charset="us-ascii"
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Message: 6 Date: Thu, 9 Mar 2006 11:35:01 -0300 (BRT) From: diogo$##$unilavras.edu.br Subject: ORGLIST: nitroarene reduction To: everybody$##$orglist.net Message-ID: <2359.150.164.110.75.1141914901.squirrel$##$webmail.unilavras.edu.br> Content-Type: text/plain;charset=iso-8859-1
Hi, everybody! There4s been a long time since I4m trying to reduce some nitro derivatives of vanillin. we aren4t able to do it by catalytic hydrigenation since we don4t have the reagent and apparatus. But I4ve been searching some methods in literature and I4m quite envolved with borohydride-transition metal nitro reduction. Besides reducting the nitro group and the formyl group (also present in the molecule) there have been many other byproducts, I guees degradation. I would appreciate if you could sugest ways to overcome this and get the pure aromatic amino and maybe even not the reducted formyl group. other reduction systems are quite welcome. Diogo
------------------------------
Message: 7 Date: Thu, 09 Mar 2006 18:01:01 +0300 From: "bijster bagger" <bijster_bagger$##$hotmail.com> Subject: ORGLIST: R'-OH --> R'-NH-R" To: everybody$##$orglist.net Message-ID: <BAY22-F685675B470E6314EE0889F5EC0$##$phx.gbl> Content-Type: text/plain; format=flowed
Dear fellow chemists,
I've been trying to convert an alcohol to a secundairy amine, and found the following in Vogel (5th ed), p. 779:
"A similar ammonolysis of alcohols in the prescence of certain metallic oxide catalysts is, however, extensively used on the large scale for the manufacture of all classes of amines."
This refers to the following condensation reaction :
R'-OH + R"-NH2 --> R'-NH-R" + H2O
Further searching did not yield any more information about this process. Can anybody suggest which metallic oxide catalyst can be used, and under which process conditions? And, if at all possible, supply me with some references?
Thanks in advance,
Reni The Netherlands
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Message: 8 Date: Thu, 9 Mar 2006 09:00:13 -0800 (PST) From: Sengen Sun <sengensun$##$yahoo.com> Subject: Re: ORGLIST: Seperation of nitro compounds To: everybody$##$orglist.net Message-ID: <20060309170013.49836.qmail$##$web53712.mail.yahoo.com> Content-Type: text/plain; charset=iso-8859-1
I recrystalized my nitration products from ethanol. I did lot of this kind of reactions about 20 years ago.
Good luck.
Sengen
--- srinivas reddy <gounisrinivas$##$yahoo.com> wrote:
> Hi, > > can anybody help me on how to seperate the mixture > of > aromatic nitro compounds that are formed by > nitration > with HNO3/H2SO4?. I tried with column chromatography > but of not much use. > > thanks in davance > > GSR > > __________________________________________________ > Do You Yahoo!? > Tired of spam? Yahoo! Mail has the best spam > protection around > http://mail.yahoo.com > _______________________________________________ > ORGLIST - Organic Chemistry Mailing List > Website / Archive / FAQ: http://www.orglist.net > To post a message (TO EVERYBODY) send to > everybody$##$orglist.net > To unsubscribe, send to > everybody-request$##$orglist.net the message: > unsubscribe your_orglist_password your_address >
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