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Protecting groups

 
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Mar17-13, 08:14 PM   #1
 

Protecting groups


Hello,

I am unsure of how to utilize protecting groups in organic synthesis problems. What would be an immediate sign to the trained eye that one should use a protecting group such as TBDMS-Cl?
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Mar17-13, 09:28 PM   #2
 
What is the purpose of protecting groups (PG)?
Mar17-13, 09:57 PM   #3
 
To protect something from being reduced completely
Mar17-13, 10:05 PM   #4
 

Protecting groups


Look for an alcohol that you want to keep in addition to a carbonyl that you want to reduce
Mar17-13, 11:03 PM   #5
 
Quote by Woopydalan View Post
To protect something from being reduced completely
  • Draw the reagents you can use for protecting different functional groups.
  • Notice the similar structures between different reagents used to protect a single functional group.
  • Identify the something (functional group) you want to protect.
  • Select a reagent you have available for protecting that functional group.
  • Push arrows.

Here is wiki's list of functional groups and their protecting groups:
http://en.wikipedia.org/wiki/Protecting_group

When I see TBDMS-Cl, I see a radical Cl anion waiting to react with an acidic hydrogen,usually in a hydroxyl group.
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