December 22, 2024, 08:34:00 PM
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Topic: Morpholine ring closure  (Read 2364 times)

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Offline bcoots

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Morpholine ring closure
« on: February 22, 2013, 11:04:18 AM »
I would like to make an N-alkyl Morpholine. There is a literature method that uses N-alkyl amine plus dichloroethyl ether.

I would like to avoid using this chlorinated raw material, and wondered if an N-alkyl diethanolamine could be dehydrated to give the morpholine ring.

Any ideas?

Offline Arkcon

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Re: Morpholine ring closure
« Reply #1 on: February 22, 2013, 11:10:46 AM »
Your plan seems to match the one given in Wikipedia:  http://en.wikipedia.org/wiki/Morpholine#Production And there is also a reference given there if it helps you understand how its done even better.
Hey, I'm not judging.  I just like to shoot straight.  I'm a man of science.

Offline Dan

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Re: Morpholine ring closure
« Reply #2 on: February 22, 2013, 11:13:03 AM »
What is R?

I would consider reductive amination of carbonyls with morpholine - but it depends on what R is.
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Offline bcoots

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Re: Morpholine ring closure
« Reply #3 on: February 22, 2013, 04:05:12 PM »
Dan - R is an alkyl group derived from a C18 fatty acid.

Offline Dan

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Re: Morpholine ring closure
« Reply #4 on: February 23, 2013, 06:05:14 AM »
Then I would probably do one of two things:

1. Make the corresponding "fatty acid aldehyde" and reductively aminate it with morpholine or...
2. Couple the fatty acid with morpholine and reduce the resulting amide to the amine.

The second option is probably the easier one.
My research: Google Scholar and Researchgate

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