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Topic: crownethers  (Read 4043 times)

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Offline revathikala

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crownethers
« on: March 21, 2008, 02:40:36 AM »
Hi,
Iam working on crownethers preparation,but i have lot of doubts in preparation of crown ethers.In the preparation of crownethers iam facing the solubility problem during the reaction.I am using dry THF as a reaction medium & continued the reaction for 21hrs.At the middle of the reaction total Dry THF evaporated & the total reaction mixture becomes solid because of evaporating Dry THF.Starting material of my reaction is tetrahydroxy compound & iam preparing dicrown compound from this.Please suggest any reaction medium & information on crownethers preparation.

My reaction is as follows
        MY starting material is symmetrical tetra hydroxy compound ,I want to
prepare bis15-crown-5 compound.For this preparation of dicrown i did reaction between tetrahydroxy compound & TEG ditosylate in presence of Dry THF & NaH under nitrogen presence.But the reaction is not going on  & i faced So many problems.Thats why Plese suggest any reaction or medium or conditoinsthat are used during the reaction to forward my step for preparation of dicrown.

thanking you.
« Last Edit: May 02, 2008, 07:14:53 AM by revathikala »

Offline AWK

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Re: crownethers
« Reply #1 on: March 21, 2008, 03:21:35 AM »
There are many crown ethers, and they need different reaction conditions for synthesis. Usually you use a known procedure for a specific crown ether, and it should be work. Just read it carefully.

Using your secret data nobody can help you. Dicrowns may be much more difficult for synthesis. There is a bulk of literature on this subject.
AWK

Offline DrCMS

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Re: crownethers
« Reply #2 on: March 21, 2008, 07:57:12 AM »
How are you carrying out the reaction, conditions and equipment?
Why does your THF evaporate?

Offline agrobert

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Re: crownethers
« Reply #3 on: March 21, 2008, 11:52:58 AM »
You should cover your reaction so it doesn't evaporate.  Keep it under positive pressure of Argon or Nitrogen.
In the realm of scientific observation, luck is only granted to those who are prepared. -Louis Pasteur

Offline revathikala

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Re: crownethers
« Reply #4 on: March 24, 2008, 03:19:16 AM »
SIR ,i gave in detail of my reaction .see once & say any suggestion

Offline AWK

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Re: crownethers
« Reply #5 on: March 25, 2008, 02:14:28 AM »
As I know, tosylates are used for reactions with amines mainly.

For synthesis you probably need a very diluted solutions.

Are you sure you use a tetrahydroxycompound?
AWK

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