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ibeza4

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Everything posted by ibeza4

  1. Ah, good idea. I think this might be more of what the professor is looking for. I'll see what she thinks. Thank you very much
  2. Hmm that sounds like another possibility, but I can tell you we never covered that in class, or even the stuff I posted. I found the Sono coupling online. There must be a more basic way. I do appreciate the response, UC.
  3. aka: isopropylphenylacetylene I have an idea how to get this, but it may be wrong or there may be an easier way to get to the product. The guidelines are: may only use benzene, acohols, alkyl halides with 3 carbons or less, and inorganic reagents can be used. I have a feeling there is an easier way since we don't even get into dehydrogenations and Sonogashira couplings in orgo2. This is what I have: 1) Benzene + CH3CH2CL ->ALCL3-> to give ethylbenzene 2) dyhydrogenation performed to give ethenylbenzene 3) addition of Br2 to give (1,2-Dibromoethyl)-benzene 4) NaNH2 in lquid ammonia to give phenyl acetylene 5) Sonogashira Coupling performed with 2-bromopropane to give the final product Thank you for any help that anyone can give.
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