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Topic: Triethyl orthoacrylate  (Read 1400 times)

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Offline AlphaScent

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Triethyl orthoacrylate
« on: February 04, 2019, 11:55:18 AM »
Hey All,

I understand that this compound may be reactive, but to not find it on any of the big chemical suppliers is odd.  Any input?
I am trying to reference a reaction from ACIE 2007, 46, 7458.  The paper itself references JOC 1982, 47, 946.

The ACIE paper uses triethyl orthoacrylate.  I would hate to have to make it..

Any input helps.

Cheers!
If you're not part of the solution, then you're part of the precipitate

Offline wildfyr

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Re: Triethyl orthoacrylate
« Reply #1 on: February 04, 2019, 01:31:03 PM »
Are you willing to use the methyl? It's commonly available.

Offline AWK

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Re: Triethyl orthoacrylate
« Reply #2 on: February 04, 2019, 02:38:33 PM »
check for:
3,3,3-Triethoxy-1-propene
AWK

Offline AlphaScent

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Re: Triethyl orthoacrylate
« Reply #3 on: February 05, 2019, 01:31:03 PM »
wildfyr,

Where is it commonly available?  Can you tell me a source?  I cant seem to fine the methyl on Sigma, AKsci, or Oakwood.

AWK,

I did look under the IUPAC name as well!  No luck.

Cheers,
If you're not part of the solution, then you're part of the precipitate

Offline wildfyr

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Re: Triethyl orthoacrylate
« Reply #4 on: February 05, 2019, 02:01:41 PM »
I totally missed the acrylate part. I was thinking trimethyl orthoformate.
« Last Edit: February 05, 2019, 07:47:08 PM by wildfyr »

Offline AWK

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Re: Triethyl orthoacrylate
« Reply #5 on: February 05, 2019, 02:58:19 PM »
AWK

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